First Example of the Solid-State Thermal Cyclometalation of Ligated

Inorg. Chem. 2007, 46, 4469−4482

First Example of the Solid-State Thermal Cyclometalation of Ligated Benzophenone Imine Giving Novel Luminescent Platinum(II) Species Yulia Yu. Scaffidi-Domianello,†,‡ Alexey A. Nazarov,† Matti Haukka,§ Markus Galanski,*,† Bernhard K. Keppler,† Jacob Schneider,| Pingwu Du,| Richard Eisenberg,*,| and Vadim Yu. Kukushkin*,‡ Institute of Inorganic Chemistry, UniVersity of Vienna, Wa¨hringerstrasse 42, A-1090 Vienna, Austria, Department of Chemistry, St. Petersburg State UniVersity, 198504 Stary Petergof, Russian Federation, Department of Chemistry, UniVersity of Joensuu, P.O. Box 111, FI-80101 Joensuu, Finland, and Department of Chemistry, UniVersity of Rochester, Rochester, New York 14627 Received December 16, 2006

The (benzophenone imine)platinum(II) compounds trans-[PtCl2(Ph2CdNH)(RR′SO)] [R, R′ ) Me, Me (2); n-Pr, nPr (3); (CH2)4 (4); Me, Ph (5); Me, p-MeC6H4 (6)] were prepared by the reaction of Ph2CdNH with K[PtCl3(RR′SO)], obtained in situ from K2[PtCl4] and the corresponding sulfoxide, giving 2−6 as well as cis-[PtCl2(Ph2CdNH)2] (1) as a minor product. The complexes were characterized by 1H, 13C, and 195Pt NMR and IR spectroscopy, electrospray ionization mass spectrometry, and C, H, and N elemental analysis. The X-ray crystallography of 1 enables confirmation of the cis configuration of the complex, while in 2 and 4‚1/2CHCl3, the imine and sulfoxide ligands are mutually trans. The solid-state structure of 4‚1/2CHCl3 consists of two dimeric Pt moieties representing a rather weak Pt‚‚‚Pt interaction. The dimeric architecture of 4‚1/2CHCl3 is enhanced by the hydrogen bonding between imine H atoms and O atoms. The orthometalation of 1 and 2−6 proceeds both in the solid phase and in a toluene suspension, leading to the formation of [PtCl{Ph(C6H4)CdNH}(Ph2CdNH)] (7) and [PtCl{Ph(C6H4)CdNH}(RR′SO)] (8−12), respectively, isolated in nearly quantitative yields. Complexes 8−12 are emissive at room temperature both in max solution (λmax em ∼535 nm) and in the solid state (λem 560−610 nm), with excited-state lifetimes of ca. 300−600 ns, II representing a new family of Pt -based luminescent complexes. Compounds 8 and 10 have been characterized by X-ray analysis, confirming the square-planar coordination geometry of the metal center with the almost planar platinacycles. In 8, the asymmetric unit contains two independent Pt molecules, while in 10, it includes four Pt molecules linked by the intermolecular hydrogen-bonding network between the NH group and Cl atoms.

Introduction In the recent years, there has been an increasing interest in metal-mediated synthesis, properties, and reactivity patterns of ligated imines.1 Unlike N-substituted imines R′Nd CR2 (R′ ) Alk, Ar; R ) H, Alk, Ar), which are mostly stable and serve as ligands for many metal complexes,2 the unsubstituted aldimines or ketimines HNdCR2 are, with the exception of diarylketimines, very susceptible to hydrolysis and subject to oligo- and polymerization and various redox* To whom correspondence should be addressed. E-mail: [email protected] (M.G.), [email protected] (R.E.), [email protected] (V.Yu.K.). † University of Vienna. ‡ St. Petersburg State University. § University of Joensuu. | University of Rochester.

10.1021/ic062414k CCC: $37.00 Published on Web 04/24/2007

© 2007 American Chemical Society

type conversions.3 However, they can be stabilized via coordination to a metal center; in particular, Pt group metals provide enormous stabilization of the potentially unstable imines.4-9 Metal imine species are the subject of rapt attention because of the importance of their potential properties, i.e., (i) PtII complexes containing coordinated acetimine display a tumor cell growth inhibitory potency, similar to that of (1) (a) Vicente, J.; Chicote, M.-T.; Abrisqueta, M.-D.; Guerrero, R.; Jones, P. G. Angew. Chem., Int. Ed. Engl. 1997, 36, 1203. (b) Vicente, J.; Chicote, M.-T.; Guerrero, R.; Saura-Llamas, I. M.; Jones, P. G.; Ramı´rez de Arellano, M. C. Chem.sEur. J. 2001, 7, 638. (c) Vicente, J.; Chicote, M.-T.; Guerrero, R.; Vicente-Hernańdez, I.; Jones, P. G. Inorg. Chem. 2003, 42, 7644. (d) Vicente, J.; Chicote, M.-T.; Guerrero, R.; Vicente-Hernańdez, I.; Alvarez-Falcoń, M. M. Organometallics 2005, 24, 4506. (e) Vicente, J.; Chicote, M.-T.; Guerrero, R.; VicenteHernańdez, I.; Alvarez-Falcoń, M. M. Inorg. Chem. 2006, 45, 181.

Inorganic Chemistry, Vol. 46, No. 11, 2007

4469

Scaffidi-Domianello et al. PtII

10

the corresponding complexes with iminoethers, and in addition the ability to circumvent (either partially or completely) cisplatin resistance;11 (ii) ytterbium(II) imine complexes exhibit a high catalytic activity in the dehydrogenative silylation of terminal alkynes12a and hydrosilylation of imines;12b (iii) metal complexes of simple imines are observed/proposed to be intermediates in the metal-mediated imine aziridination,13 imine/imide/alkylidene metathesis,14 and amine T nitrile interconversion;15 (iv) R,R-diimines in (2) Mehrotra, R. C. ComprehensiVe Coordination Chemistry; Pergamon: Oxford, U.K., 1987; Vol. 2. (3) Robertson, G. M. Imines and Their N-Substituted DeriVatiVes: NH, N-R and N-Haloimines; Pergamon: Oxford, U.K., 1995; Vol. 3. (4) (a) Kukushkin, V. Yu.; Ilichev, I. V.; Wagner, G.; Frau´sto da Silva, J. J. R.; Pombeiro, A. J. L. J. Chem. Soc., Dalton Trans. 1999, 3047. (b) Kukushkin, V. Yu.; Ilichev, I. V.; Zhdanova, M. A.; Wagner, G.; Pombeiro, A. J. L. J. Chem. Soc., Dalton Trans. 2000, 1567. (5) (a) Kukushkin, V. Yu.; Pakhomova, T. B.; Kukushkin, Yu. N.; Herrmann, R.; Wagner, G.; Pombeiro, A. J. L. Inorg. Chem. 1998, 37, 6511. (b) Makarycheva-Mikhailova, A. V.; Haukka, M.; Bokach, N. A.; Garnovskii, D. A.; Galanski, M.; Keppler, B. K.; Pombeiro, A. J. L.; Kukushkin, Yu, V. New J. Chem. 2002, 26, 1085. (c) Kukushkin, V. Yu.; Pakhomova, T. B.; Bokach, N. A.; Wagner, G.; Kuznetsov, M. L.; Galanski, M.; Pombeiro, A. J. L. Inorg. Chem. 2000, 39, 216. (6) (a) Luzyanin, K. V.; Kukushkin, V. Yu.; Kuznetsov, M. L.; Garnovskii, D. A.; Haukka, M.; Pombeiro, A. J. L. Inorg. Chem. 2002, 41, 2981. (b) Wagner, G.; Pakhomova, T. B.; Bokach, N. A.; Frau´sto da Silva, J. J. R.; Vicente, J.; Pombeiro, A. J. L.; Kukushkin, V. Yu. Inorg. Chem. 2001, 40, 1683. (7) Bokach, N. A.; Kukushkin, V. Yu.; Kuznetsov, M. L.; Garnovskii, D. A.; Natile, G.; Pombeiro, A. J. L. Inorg. Chem. 2002, 41, 2041. (8) Ferreira, C. M. P.; Guedes da Silva, M. F. C.; Frau´sto da Silva, J. J. R.; Pombeiro, A. J. L.; Kukushkin, V. Yu.; Michelin, R. A. Inorg. Chem. 2001, 40, 1134. (9) (a) Bokach, N. A.; Kukushkin, V. Yu.; Haukka, M.; Frau´sto da Silva, J. J. R.; Pombeiro, A. J. L. Inorg. Chem. 2003, 42, 3602. (b) Garnovskii, D. A.; Kukushkin, V. Yu.; Haukka, M.; Wagner, G.; Pombeiro, A. J. L. J. Chem. Soc., Dalton Trans. 2001, 560. (c) Kukushkin, V. Yu.; Pombeiro, A. J. L. Chem. ReV. 2002, 102, 1771. (10) (a) Coluccia, M.; Nassi, A.; Loseto, F.; Boccarelli, A.; Mariggio, M. A.; Giordano, D.; Intini, F. P.; Caputo, P.; Natile, G. J. Med. Chem. 1993, 36, 510. (b) Novakova, O.; Kasparkova, J.; Malina, J.; Natile, G.; Brabec, V. Nucleic Acids Res. 2003, 31, 6450 and references cited therein. (11) Boccarelli, A.; Intini, F. P.; Sasanelli, R.; Sivo, M. F.; Coluccia, M.; Natile, G. J. Med. Chem. 2006, 49, 829. (12) (a) Takaki, K.; Kurioka, M.; Kamata, T.; Takehira, K.; Makioka, Y.; Fujiwara, Y. J. Org. Chem. 1998, 63, 9265. (b) Takaki, K.; Kamata, T.; Miura, Y.; Shishido, T.; Takehira, K. J. Org. Chem. 1999, 64, 3891. (13) (a) Rasmussen, K. G.; Hazell, R. G.; Jørgensen, K. A. Chem. Commun. 1997, 1103. (b) Rasmussen, K. G.; Juhl, K.; Hazell, R. G.; Jørgensen, K. A. J. Chem. Soc., Perkin Trans. 2 1998, 1347. (14) Cantrell, G. K.; Meyer, T. Y. J. Am. Chem. Soc. 1998, 120, 8035. (15) (a) Diamond, S. E.; Tom, G. M.; Taube, H. J. Am. Chem. Soc. 1975, 97, 2661. (b) Keene, F. R.; Salmon, D. J.; Meyer, T. J. J. Am. Chem. Soc. 1976, 98, 1884. (c) Gunnoe, T. B.; White, P. S.; Templeton, J. L. J. Am. Chem. Soc. 1996, 118, 6916. (16) (a) Fedushkin, I. L.; Skatova, A. A.; Chudakova, V. A.; Fukin, G. K. Angew. Chem., Int. Ed. 2003, 42, 3294. (b) Fedushkin, I. L.; Skatova, A. A.; Chudakova, V. A.; Fukin, G. K.; Dechert, S.; Schumann, H. Eur. J. Inorg. Chem. 2003, 3336. (c) Fedushkin, I. L.; Khvoinova, N. M.; Skatova, A. A.; Fukin, G. K. Angew. Chem., Int. Ed. 2003, 42, 5223. (d) Fedushkin, I. L.; Skatova, A. A.; Cherkasov, V. K.; Chudakova, V. A.; Dechert, S.; Hummert, M.; Schumann, H. Chem.s Eur. J. 2003, 9, 5778. (e) Fedushkin, I. L.; Skatova, A. A.; Hummert, M.; Schumann, H. Eur. J. Inorg. Chem. 2005, 1601. (f) Fedushkin, I. L.; Skatova, A. A.; Fukin, G. K.; Hummert, M.; Schumann, H. Eur. J. Inorg. Chem. 2005, 2332. (g) Fedushkin, I. L.; Morozov, A. G.; Rassadin, O. V.; Fukin, G. K. Chem.sEur. J. 2005, 11, 5749. (h) Fedushkin, I. L.; Chudakova, V. A.; Skatova, A. A.; Fukin, G. K. Heteroatom Chem. 2005, 16, 633. (i) Fedushkin, I. L.; Makarov, V. M.; Rosenthal, E. C. E.; Fukin, G. K. Eur. J. Inorg. Chem. 2006, 827.

4470 Inorganic Chemistry, Vol. 46, No. 11, 2007

their main-group metal complexes may possess different oxidation states, thus acting as an electron sponge or sink toward organic substrates;16 (v) PdII- and NiII-based catalysts containing bulky diimine ligands exhibit extremely high activities in the conversion of ethylene,17a-c R-olefins,17a,b,d cyclopentene,17e and trans-1,2-disubstituted olefins17f to high-molecular-weight polymers with unique microstructures as well as in copolymerization of polar monomers with ethylene and R-olefins.17g,h Therefore, synthetic approaches to new arylimine metal complexes as well as examination of their reactivity are crucial for the development of that type of compound and to a considerable degree determinative for the progress of metal-mediated arylimine functionalization. In view of our general interest in imines as ligands4-9 and ligand reactivity in general,18 we continued our work in these directions and focused our attention on a rather stable and commercially available imine, i.e., benzophenone imine, HNdCPh2, which can be considered as a model for unstable imines in examinations of their reactivity. Although coordination properties of HNdCPh2 were extensively studied, e.g., exhaustively in the case of group VIII metals (Fe,19 Ru,20 (17) (a) Johnson, L. K.; Killian, C. K.; Brookhart, M. J. Am. Chem. Soc. 1995, 117, 6414. (b) Brookhart, M. S.; Johnson, L. K.; Killian, C. M.; Arthur, S. D.; Feldman, J.; McCord, E. F.; McLain, S. J.; Kreutzer, K. A.; Bennett, M. A.; Coughlin, E. B.; Ittel, S. D.; Parthasarathy, A.; Tempel, D. J. WO 9623010, 1996. (c) Gates, D. P.; Svejda, S. A.; Onãte, E.; Killian, C. M.; Johnson, L. K.; White, P. S.; Brookhart, M. Macromolecules 2000, 33, 2320. (d) Killian, C. M.; Tempel, D. J.; Johnson, L. K.; Brookhart, M. J. Am. Chem. Soc. 1996, 118, 11664. (e) McLain, S. J.; Feldman, J.; McCord, E. F.; Gardner, K. H.; Teasley, M. F.; Coughlin, E. B.; Sweetman, K. J.; Johnson, L. K.; Brookhart, M. Macromolecules 1998, 31, 6705. (f) Leatherman, M. D.; Brookhart, M. Macromolecules 2001, 34, 2748. (g) Johnson, L. K.; Mecking, S.; Brookhart, M. J. Am. Chem. Soc. 1996, 118, 267. (h) Mecking, S.; Johnson, L. K.; Wang, L.; Brookhart, M. J. Am. Chem. Soc. 1998, 120, 888. (18) (a) Bokach, N. A.; Kuznetsova, T. V.; Simanova, S. A.; Haukka, M.; Pombeiro, A. J. L.; Kukushkin, V. Yu. Inorg. Chem. 2005, 44, 5152. (b) Bokach, N. A.; Kukushkin, V. Yu.; Haukka, M.; Pombeiro, A. J. L. Eur. J. Inorg. Chem. 2005, 845. (c) Luzyanin, K. V.; Kukushkin, V. Yu.; Haukka, M.; Frausto da Silva, J. J. R.; Pombeiro, A. J. L. J. Chem. Soc., Dalton Trans. 2004, 2728. (d) Garnovskii, D. A.; Pombeiro, A. J. L.; Haukka, M.; Sobota, P.; Kukushkin, V. Yu. J. Chem. Soc., Dalton Trans. 2004, 1097. (e) Pombeiro, A. J. L.; Kukushkin, V. Yu. ComprehensiVe Coordination Chemistry II; Elsevier Ltd.: Oxford, U.K., 2004; Vol. 1. (f) Makarycheva-Mikhailova, A. V.; Bokach, N. A.; Haukka, M.; Kukushkin, V. Yu. Inorg. Chim. Acta 2003, 356, 382. (g) Kopylovich, M. N.; Pombeiro, A. J. L.; Fischer, A.; Kloo, L.; Kukushkin, V. Yu. Inorg. Chem. 2003, 42, 7239. (h) Ferreira, C. M. P.; Guedes da Silva, M. F. C.; Michelin, R. A.; Kukushkin, V. Yu.; Frausto da Silva, J. J. R.; Pombeiro, A. J. L. J. Chem. Soc., Dalton Trans. 2003, 3751. (i) Charmier, M. A. J.; Kukushkin, V. Yu.; Pombeiro, A. J. L. J. Chem. Soc., Dalton Trans. 2003, 2540. (j) Makarycheva-Mikhailova, A. V.; Bokach, N. A.; Kukushkin, V. Yu.; Kelly, P. F.; Gilby, L. M.; Kuznetsov, M. L.; Holmes, K. E.; Haukka, M.; Parr, J.; Stonehouse, J. M.; Elsegood, M. R. J.; Pombeiro, A. J. L. Inorg. Chem. 2003, 42, 301. (19) Busetto, L.; Marchetti, F.; Zacchini, S.; Zanotti, V.; Zoli, E. J. Organomet. Chem. 2005, 690, 348. (20) (a) Bohanna, C.; Esteruelas, M. A.; Lo´pez, A. M.; Oro, L. A. J. Organomet. Chem. 1996, 526, 73. (b) Esteruelas, M. A.; Go´mez, A. V.; Lahoz, F. J.; Lo´pez, A. M.; Onãte, E.; Oro, L. A. Organometallics 1996, 15, 3423. (c) Andreu, P. L.; Cabeza, J. A.; del Rıó, I.; Riera, V. Organometallics 1996, 15, 3004. (d) Jimeńez-Tenorio, M. A.; JimeńezTenorio, M.; Puerta, M. C.; Valerga, P. Inorg. Chim. Acta 2000, 300302, 869. (e) Jimeńez-Tenorio, M.; Palasios, M. D.; Puerta, M. C.; Valerga, P. J. Organomet. Chem. 2004, 689, 2776. (f) Huang, J.-S.; Leung, S. K.-Y.; Zhou, Z.-Y.; Zhu, N.; Che, C.-M. Inorg. Chem. 2005, 44, 3780.

Cyclometalation of Ligated Benzophenone Imine

Os;21 Co,22 Rh,23 Ir;23a Ni,24 Pd,25 Pt9b,26) and partially for some representatives of group III (Sm27), IV (Ti,28 Zr28,29), VI (Cr30), and VII (Mn,31 Re31,32) metals, reports on the reactiVity of the metal-bound HNdCPh2 are rather scarce. Thus, several papers devoted to its deprotonation, resulting in the formation of azavinylidene complexes,21a,b the addition of tolylacetilyde to the coordinated HNdCPh2,19 and the formation of ligated σ-η1-C6H4C(Ph)dNH species, were published.20d In this context, also a few reports on the orthometalation of the coordinated HNdCPh2 species leading to N,C-chelates, performed in most cases in toluene or tetrahydrofuran solutions at elevated temperatures, are available.20c,21c,h,j,22,23d,26 Herein, we report on the preparation of (benzophenone imine)(sulfoxide)platinum(II) complexes. The reactivity of the HNdCPh2 ligand both in the solid state and in a toluene suspension, leading to the formation of the corresponding orthometalated species exhibiting luminescent properties, was studied. It is worth emphasizing that within the framework of this project we observed for the first time the solid-state reactiVity of the coordinated benzophenone imine, namely, the formation of a platinacycle via elimination of HCl upon heating of the solid platinum(II) imine complexes. (21) (a) Thomas, D.; Werner, H. Z. Naturforsch., B: Chem. Sci. 1992, 47, 1707. (b) Thomas, D.; Knaup, W.; Dziallas, M.; Werner, H. Chem. Ber. 1993, 126, 1981. (c) Esteruelas, M. A.; Lahoz, F. J.; Lo´pez, A. M.; Onãte, E.; Oro, L. A. Organometallics 1995, 14, 2496. (d) Albeńiz, M. J.; Buil, M. L.; Esteruelas, M. A.; Lo´pez, A. M. J. Organomet. Chem. 1997, 545-546, 495. (e) Barea, G.; Esteruelas, M. A.; Lledo´s, A.; Lo´pez, A. M.; Tolosa, J. I. Inorg. Chem. 1998, 37, 5033. (f) Barea, G.; Esteruelas, M. A.; Lledo´s, A.; Lo´pez, A. M.; Onãte, E.; Tolosa, J. I. Organometallics 1998, 17, 4065. (g) Esteruelas, M. A.; Gutie´rrez-Puebla, E.; Lo´pez, A. M.; Onãte, E.; Tolosa, J. I. Organometallics 2000, 19, 275. (h) Cabeza, J. A.; del Rıó, I.; Grepioni, F.; Riera, V. Organometallics 2000, 19, 4643. (i) Aime, S.; Diana, E.; Gobetto, R.; Milanesio, M.; Valls, E.; Viterbo, D. Organometallics 2002, 21, 50. (j) Esteruelas, M. A.; Lledo´s, A.; Olivań, M.; Onãte, E.; Tajada, M. A.; Ujaque, G. Organometallics 2003, 22, 3753. (22) Klein, H.-F.; Camadanli, S.; Beck, R.; Leukel, D.; Flo¨rke, U. Angew. Chem., Int. Ed. 2005, 44, 975. (23) (a) Esteruelas, M. A.; Lahoz, F. J.; Olivań, M.; Onãte, E.; Oro, L. A. Organometallics 1994, 13, 3315. (b) Fryzuk, M. D.; Piers, W. E. Organometallics 1990, 9, 986. (c) Zhao, P.; Hartwig, J. F. J. Am. Chem. Soc. 2005, 127, 11618. (d) Ezhova, M. B.; Patrick, B. O.; James, B. R. Organometallics 2005, 24, 3753. (24) Hoberg, H.; Goetz, V.; Krueger, C.; Tsay, Y. H. J. Organomet. Chem. 1979, 169, 209. (25) (a) Ruiz, J.; Rodrı´guez, V.; Cutillas, N.; Florenciano, F.; Pe´rez, J.; Lo´pez, G. Inorg. Chem. Commun. 2001, 4, 23. (b) Kuwabara, J.; Takeuchi, D.; Osakada, K. Bull. Chem. Soc. Jpn. 2005, 78, 668. (26) Grøndahl, L.; Josefsen, J.; Bruun, J. M.; Larsen, S. Acta Chem. Scand. 1999, 53, 1069. (27) (a) Koizumi, T.-A.; Yoda, C.; Hou, Z.; Fukuzawa, S.-I.; Wakatsuki, Y. Jpn. Kidorui 1999, 34, 284. (b) Hou, Z.; Yoda, C.; Koizumi, T.A.; Nishiura, M.; Wakatsuki, Y.; Fukuzawa, S.-I.; Takats, J. Organometallics 2003, 22, 3586. (28) Lefeber, C.; Arndt, A.; Tillack, A.; Baumann, W.; Kempe, R.; Burlakov, V. V.; Rosenthal, U. Organometallics 1995, 14, 3090. (29) Ho¨ltke, C.; Erker, G.; Kehr, G.; Fro¨hlich, R.; Kataeva, O. Eur. J. Inorg. Chem. 2002, 2789. (30) Campos, P. J.; Sampedro, D.; Rodrı´gez, M. A. Organometallics 2000, 19, 3082. (31) Terry, M. R.; Mercando, L. A.; Kelley, C.; Geoffroy, G. L. Organometallics 1994, 13, 843. (32) Cabeza, J. A.; del Rıó, I.; Zun˜iga-Villareal, N.; Garcıá-Granda, S. Acta Crystallogr. 2001, E57, m130. (33) (a) Shilov, A. E.; Shul’pin, G. B. Chem. ReV. 1997, 97, 2879. (b) Ryabov, A. D. Chem. ReV. 1990, 90, 403.

Results and Discussion In general, the orthometalation reactionsactivation of a C-H bond in the ortho position of an aromatic ring by a transition-metal centerscontinues to be an important class of reactions33 owing to the broad application spectrum of the orthometalated species, e.g., in catalysis,33b,34 organic synthesis,35 and material science.36 The activation of C-H bonds by transition-metal compounds is of general interest because of the possibility of functionalizing nonactivated organic molecules.33a,37 For instance, the Murai reaction,38 which represents one of the most important processes in organic synthesis, allows the alkylation of aromatic ketones,39 esters,40 and imines,41 as well as the copolymerization of aromatic ketones and R,ω-divinylsilanes.42 Consequently, stable and structurally characterized compounds containing N,C-metallacycles are of high interest and can be considered as models for the organometallic intermediates in C-C coupling reactions between aromatic imines and olefins.43 Orthometalation of PtII compounds with N-donor ligands giving N,C-platinacycles is rather well documented.44 However, there are only a few examples of orthoplatinated imino species.26,45 In addition to mononuclear platinacycles with η2-coordinated imines,26,45e,i some PtII complexes with C,N,S45a and C,N,N-45d,g,j pincer ligands, orthoplatinated heterocyclederived imino species,45b and bridged45c,h and tetrameric orthometalated PtII compounds45f obtained as a result of metalation of a PtII-bound imine were reported. Thus, we have focused on the study of cyclometalation of (Ph2CdNH)PtII species and intended (i) to prepare PtII complexes with both benzophenone imine and various sulfoxides, (ii) to investigate the solid-state and solution reactivities of (Ph2CdNH)PtII species, (iii) to verify possible routes for cyclometalation of (Ph2CdNH)PtII complexes, and (iv) to study properties of the cyclomelatated species. The report on our experiments given below follows these lines. (34) Trzeciak, A. M.; Zio´łowski, J. J. Organomet. Chem. 2000, 597, 69. (35) Ryabov, A. D. Synthesis 1985, 233. (36) (a) Cocchi, M.; Virgili, D.; Sabatini, C.; Fattori, V.; Di Marko, P.; Maestri, M.; Kalinowski, J. Synth. Met. 2004, 147, 253. (b) Maestri, M.; Sandrini, D.; Balzani, V.; Maeder, U.; von Zelewsky, A. Inorg. Chem. 1987, 26, 1323. (c) Didier, P.; Ortmans, I.; Kirsch-De Mesmaeker, A.; Watts, R. J. Inorg. Chem. 1993, 32, 5239. (d) Di Bella, S.; Fragali, I.; Ledoux, I.; Diaz-Garcia, M. A.; Marks, T. J. J. Am. Chem. Soc. 1997, 119, 9550. (e) Buey, J.; Coco, S.; Diez, L.; Espinet, P.; Martin-Alvarez, J. M.; Miguel, J. A.; Garcia-Granda, S.; Tesouro, A.; Ledoux, I.; Zyss, J. Organometallics 1998, 17, 1750. (f) Aiello, I.; Crispini, A.; Ghedini, M.; La Deda, M.; Barigelletti, F. Inorg. Chim. Acta 2000, 308, 121. (37) (a) Jia, C.; Kitamura, T.; Fujiwara, Y. Acc. Chem. Res. 2001, 34, 633. (b) Ritleng, V.; Sirlin, C.; Pfeffer, M. Chem. ReV. 2002, 102, 1731. (38) Murai, S.; Kakiuchi, F.; Sekine, S.; Tanaka, Y.; Kamatani, A.; Sonoda, M.; Chatani, N. Nature 1993, 366, 529. (39) (a) Kakiuchi, F.; Sekine, S.; Tanaka, Y.; Kamatani, A.; Sonoda, M.; Chatani, N.; Murai, S. Bull. Chem. Soc. Jpn. 1995, 68, 62. (b) Murai, S.; Chatani, N.; Kakiuchi, F. Pure Appl. Chem. 1997, 69, 589. (40) Sonoda, M.; Kakiuchi, F.; Kamatani, A.; Chatani, N.; Murai, S. Chem. Lett. 1996, 109. (41) Kakiuchi, F.; Yamauchi, M.; Chatani, N.; Murai, S. Chem. Lett. 1996, 111. (42) (a) Guo, H.; Weber, W. P. Polym. Bull. 1994, 32, 525. (b) Tapsak, M. A.; Guo, H.; Weber, W. P. Polym. Bull. 1995, 34, 49. (c) Guo, H.; Wang, G.; Tapsak, M. A.; Weber, W. P. Macromolecules 1995, 28, 5686. (43) Kakiuchi, F.; Murai, S. Acc. Chem. Res. 2002, 35, 826.


4471

Scaffidi-Domianello et al. Scheme 1

Synthesis, Characterization, and X-ray Structure Determinations of (Benzophenone imine)platinum(II) Complexes. As starting materials for the preparation of (benzophenone imine)platinum(II) compounds, we addressed the easily accessible complexes K[PtCl3(sulfoxide)]46 [sulfoxide ) Me2SO, n-Pr2SO, (CH2)4SO, racemic mixture of Me(Ph)SO, S-(-)-p-MeC6H4(Me)SO] for the following reasons: on the one hand, a significant trans effect of S-coordinated sulfoxides47 facilitates the substitution and directs the reaction to the formation of the isomerically pure product; on the other hand, as far as Me2SO is concerned, the coordinated dimethyl sulfoxide ligand with its characteristic spectral pattern48 serves as an “internal” reference for the integration of 1H NMR spectra. (44) For recent works, see: (a) Janzen, D. E.; Mehne, L. F.; Van Derveer, D. G.; Grant, G. J. Inorg. Chem. 2005, 44, 8182. (b) Otto, S.; Samuleev, P. V.; Polyakov, V. A.; Ryabov, A. D.; Elding, L. I. J. Chem. Soc., Dalton Trans. 2004, 3662. (c) Bennett, J.; David Rae, A.; Salem, G.; Ward, N. C.; Waring, P.; Wells, K.; Willis, A. C. J. Chem. Soc., Dalton Trans. 2002, 234. (d) Cave, G. W. V.; Fanizzi, F. P.; Deeth, R. J.; Errington, W.; Rourke, J. P. Organometallics 2000, 19, 1355. (e) Cardenas, D. J.; Echavarren, A. M.; Ramirez de Arellano, M. C. Organometallics 1999, 18, 3337. (f) Steenwinkel, P.; Kooijman, H.; Smeets, W. J. J.; Spek, A. L.; Grove, D. M.; van Koten, G. Organometallics 1998, 17, 5411. (g) Krooglyak, E. V.; Kazankov, G. M.; Kurzeev, S. A.; Polyakov, V. A.; Semenov, A. N.; Ryabov, A. D. Inorg. Chem. 1996, 35, 4804. (h) Kawamoto, T.; Nagasawa, I.; Kuma, H.; Kushi, Y. Inorg. Chem. 1996, 35, 2427. (i) Casas, J. M.; Fornies, J.; Martin, A.; Menjon, B.; Tomas, M. J. Chem. Soc., Dalton Trans. 1995, 2949. (45) (a) Jacquot-Rousseau, S.; Khatyr, A.; Schmitt, G.; Knorr, M.; Kubicki, M. M.; Blacque, O. Inorg. Chem. Commun. 2005, 8, 610. (b) Anderson, C.; Crespo, M. J. Organomet. Chem. 2004, 689, 1496. (c) Diez, L.; Espinet, P.; Miguel, J. A.; Ros, M. B. J. Mater. Chem. 2002, 12, 3694. (d) Bravo, J.; Cativiela, C.; Navarro, R.; Urriolabeitia, E. P. J. Organomet. Chem. 2002, 650, 157. (e) Crespo, M.; Solans, X.; Font-Bardia, M. Polyhedron 1998, 17, 3927. (f) Quiroga, A. G.; Perez, J. M.; Lopez-Solera, I.; Masaguer, J. R.; Luque, A.; Roman, P.; Edwards, A.; Alonso, C.; Navarro-Ranninger, C. J. Med. Chem. 1998, 41, 1399. (g) Lopez, O.; Crespo, M.; Font-Bardia, M.; Solans, X. Organometallics 1997, 16, 1233. (h) Buey, J.; Diez, L.; Espinet, P.; Kitzerow, H.-S.; Miguel, J. A. Chem. Mater. 1996, 8, 2375. (i) Crespo, M.; Martinez, M.; Sales, J.; Solans, X.; Font-Bardia, M. Organometallics 1992, 11, 1288. (j) Anderson, C. M.; Puddephatt, R. J.; Ferguson, G.; Lough, A. J. J. Chem. Soc., Chem. Commun. 1989, 1297. (46) (a) Kukushkin, Yu. N.; Viazmenskii, Yu. E.; Zorina, L. I. Zh. Neorg. Khim. 1968, 13, 1573. (b) Kukushkin, V. Yu.; Pombeiro, A. J. L.; Ferreira, C. M. P.; Elding, L. I. Inorg. Synth. 2002, 33, 189. (c) Almeida, S. G.; Hubbard, J. L.; Farrell, N. Inorg. Chim. Acta 1992, 193, 149.


The reaction between the platinum(II) sulfoxide complexes K[PtCl3(RR′SO)] [R, R′ ) Me, Me; n-Pr, n-Pr; (CH2)4; Me, Ph; Me, p-MeC6H4], obtained in situ from K2[PtCl4] and the corresponding sulfoxide,46 and benzophenone imine Ph2CdNH proceeds in aqueous solution at room temperature and leads to the formation of trans-[PtCl2(Ph2Cd NH)(RR′SO)] (2-6; Scheme 1) obtained as paleyellow precipitates and isolated in 40-60% yields. The diiminoplatinum(II) complex cis-[PtCl2(Ph2CdNH)2] (1), prepared earlier by Grøndahl et al. via the reaction of trans-[PtCl2(CH3CN)2] with Ph2CdNH,26 is formed in all syntheses as a minor product and isolated in 6-8% yields. Complexes 1-6 were characterized by C, H, and N microanalysis, 1H, 13C{1H}, and 195Pt NMR and IR spectroscopy, electrospray ionization mass spectrometry (ESIMS), and also X-ray crystallography (for 1, 2, and 4). All compounds gave satisfactory C, H, and N elemental analyses. ESI-MS spectra displayed the fragments [M + Na]+ and [M + K]+ having isotopic patterns that were in accordance with calculated ones. The IR spectra of 1-6 showed strong-tomedium ν(CdN) [1597-1607 cm-1] and medium ν(NH) [3195-3294 cm-1] stretching vibrations. In addition, 2-6 displayed very strong ν(SdO) [1113-1134 cm-1] bands shifted vs ν(SdO) of the free sulfoxides due to S coordination.49 The structures of 1, trans-[PtCl2(Ph2CdNH)(Me2SO)] (2), and trans-[PtCl2(Ph2CdNH){(CH2)4SO}] (4) were determined by X-ray single-crystal diffraction (Table 1 and Figures 1-3). The coordination geometries of the three complexes are slightly distorted square-planar. In all three structures, the Pt atoms are located at a crystallographic inversion center. The Pt-Cl bond distances are in the range from 2.297 to 2.308 Å, and these distances agree well with those in the previously characterized plati(47) (a) Elding, L. I.; Gro¨ning, O. Inorg. Chem. 1978, 17, 1872. (b) Ducommun, Y.; Helm, L.; Merbach, A. E.; Hellquist, B.; Elding, L. I. Inorg. Chem. 1989, 28, 377. (48) Davies, J. A. AdV. Inorg. Chem. Radiochem. 1981, 24, 115. (49) Kaplan, S. F.; Kukushkin, V. Yu.; Pombeiro, A. J. L. J. Chem. Soc., Dalton Trans. 2001, 3279 and references cited therein.

Cyclometalation of Ligated Benzophenone Imine Table 1. Selected Bond Lengths (Å) and Angles (deg) for 1, 2, 4‚1/2CHCl3, 8, and 10 1 Pt1-Cl1 Pt1-Cl2 Pt1-N1 Pt1-N2 Pt1-S1 Pt1-C13 Pt2-Cl3 Pt2-Cl4 Pt2-N2 Pt2-S2 S1-O1 S2-O2 N1-C1 N2-C18 N2-C14

2.298(2) 2.291(2) 2.001(7) 2.034(6)

8

8B

2.2969(9) 2.3034(9) 2.021(3)

2

2.306(4) 2.307(4) 2.017(13)

2.302(4) 2.308(4) 2.024(13)

2.392(2)

2.395(2)

2.3925(11)

2.3864(11)

2.3808(11)

2.3971(12)

2.019(6)

2.022(6)

2.019(4)

2.016(4)

2.013(4)

2.021(4)

2.2131(9)

2.210(4)

2.215(4)

2.215(2) 2.006(9)

2.216(2) 1.978(9)

2.2063(13) 2.016(4)

2.2054(12) 2.010(4)

2.2215(12) 2.005(4)

2.2132(13) 2.001(5)

2.302(4) 2.298(4) 2.037(13) 2.222(4) 1.469(11) 1.464(11) 1.26(2) 1.30(2)

2.305(4) 2.299(4) 2.029(12) 2.208(4) 1.457(11) 1.447(11) 1.27(2) 1.26(2)

1.476(5)

1.480(5)

1.479(4)

1.474(3)

1.473(3)

1.472(4)

1.280(10)

1.282(10)

175.40(11) 79.7(2)

175.73(12) 79.4(2)

178.30(12) 80.5(18)

174.38(12) 79.2(2)

1.467(3) 1.274(10)

1.289(4)

4

4B

10A

10B

10C

10D

1.259(10)

Cl1-Pt1-Cl2 92.83(8) N1-Pt1-N2 94.1(3) N1-Pt1-S1 C13-Pt1-N1 Pt1-N1-C1 130.5(6) Pt2-N2-C18 Pt1-N2-C14 137.2(6) Cl3-Pt2-Cl4 N2-Pt2-S2

175.81(3)

176.94(15)

175.75(14)

175.66(9)

175.2(4)

176.0(4)

131.8(2)

129.0(10) 129.0(11)

131.8(11) 131.0(11)

175.81(15) 178.3(4)

176.18(15) 177.2(4)

179.7(2) 79.7(3)

num(II) chloride compounds.50 In 1, the two imino ligands are mutually cis, which is the thermodynamically stable form for the complexes having two strong π-acceptor ligands insofar as (d-d) π bonding is known to be more effective in the cis configuration.51 In 2 and 4, the imine and sulfoxide ligands are mutually trans, which is the result of a significant trans effect of sulfoxides compared to chloride ligands facilitating the formation of kinetically controlled trans isomers. In the coordinated imine, the values of the CdN bond length [1.261-1.300 Å] are similar within 3σ and correspond to the previously reported distances of the CdN double bond in the metal-bound Ph2CdNH [1.285-1.310 Å].20d,f,32 In complexes 2 and 4, the Pt-S bond distances are in the range from 2.210 to 2.222 Å, which is in good agreement with the mean values of the Pt-S bond [2.216 Å] for S-coordinated sulfoxides.52 The solid-state structure of 4 consists of two dimeric Pt moieties with the Pt‚‚‚Pt distances at 3.271 and 3.314 Å, which are less than a double van der Waals radius for Pt [1.72 × 2 ) 3.44 Å]. This case represents a rather weak interaction taking into account that the Pt‚‚‚Pt contacts in numerous examples of dimeric PtII complexes are in the range 2.7-3.4 Å; no Pt‚‚‚Pt contacts of less than 5 Å were observed for the other complexes studied in this work by X-ray crystallography.53 The dimeric architecture of 4 is enhanced by the hydrogen bonding between imine H atoms and O atoms. The N1‚‚‚O2 and N1B‚ ‚‚O2B distances are 2.995(17) and 2.952(16) Å for the first and second Pt2 moieties, respectively. These bond lengths fall into the range of typical N‚‚‚O distances when NH‚‚‚O (50) (a) Crespo, M.; Font-Bardia, M.; Granell, J.; Martıńez, M.; Solans, X. J. Chem. Soc., Dalton Trans. 2003, 3763. (b) Vicente, J.; Chicote, M.-T.; Lagunas, M.-Ch. Inorg. Chem. 1995, 34, 5441. (51) Price, J. H.; Williamson, A. N.; Schramm, R. F.; Wayland, B. B. Inorg. Chem. 1972, 11, 1280. (52) (a) Calligaris, M. Coord. Chem. ReV. 2004, 248, 351. (b) Calligaris, M.; Carugo, O. Coord. Chem. ReV. 1996, 153, 83. (53) Hambley, T. W. Inorg. Chem. 1998, 37, 3767.

178.9(2) 79.7(3)

hydrogen bonding takes place.54 The angles N1‚‚‚H1‚‚‚O2 and N1B‚‚‚H1B‚‚‚O2B are 158.0 and 160.4°, respectively. Cyclometalation of the Ligated Benzophenone Imine. For both 1 and 2-6, a thermally induced solid-state cyclometalation was observed. A thermal analysis was performed for all synthesized compounds, and the mass loss on the first step of thermal conversion, corresponding to the loss of 1 equiv of HCl, was observed when they were heated to 150-200 °C, with the heating rate being 5 °C min-1 (see Figures S1-S6 in the Supporting Information). In a preparative experiment, the yellow powders of 1-6 were heated in an open test tube at a specific temperature (see the Experimental Section) overnight, giving a bright-orange product. The evolution of HCl was detected by a pH indicator, and weight monitoring proved the loss of 1 equiv of HCl. The measurement of the NMR spectra enabled the establishment that a solid-state conversion of 1-6 into orthometalated products [PtCl{Ph(C6H4)CdNH}(Ph2Cd NH)] (7) and [PtCl{Ph(C6H4)CdNH}(RR′SO)] (8-12) (Scheme 1) took place. The yield of 8 was almost quantitative, while compounds 1 and 3-6 partially decomposed on heating and were recrystallized to obtain analytically pure samples. Along with the solid-state cyclometalation of 1-6, an analogous process was observed on heating of the compounds in a toluene suspension. The complexes 1 and 2-6 were refluxed in toluene for 12-16 h, resulting in the elimination of 1 equiv of HCl and the formation of a five-membered platinacycle. The cyclometalated products 7-12 (Scheme 1) were isolated in nearly quantitative yields. For 1, a change of the relative position of the N atoms proved to take place as a result of the cyclometalation process. It is worth noticing that 7 was obtained earlier but in rather low yield.26 (54) (a) Onoda, A.; Yamada, Y.; Doi, M.; Okamura, T.-A.; Ueyama, N. Inorg. Chem. 2001, 40, 516. (b) Szafran´ski, M.; Katrusiak, A. Chem. Phys. Lett. 2004, 391, 267.


4473

Scaffidi-Domianello et al.

Figure 1. View of complex 1 with the atomic numbering scheme. Thermal ellipsoids are drawn with 50% probability.

Figure 2. View of complex 2 with the atomic numbering scheme. Thermal ellipsoids are drawn with 50% probability.

One should mention that, although numerous examples of cyclometalation in solution were comprehensively covered in the literature,55 reactions in the solid phase were studied in much less detail. To our knowledge, only a few examples of solid-state cyclometalation were reported, i.e., the cycloplatination of dimethyl(1-naphthyl)phosphine and dimethyl(1-naphthyl)arsine,56 O-metalation of (2-alkoxyphenyl)phosphines by PtII,57 cyclometalation of triphenylphosphine (55) (a) Crespo, M.; Solans, X.; Font-Bardıá, M. Polyhedron 1998, 17, 3927. (b) Va´zques-Garcia, D.; Fernańdez, A.; Fernańdez, J. J.; Lo´pezTorres, M.; Sua´rez, A.; Ortigueira, J. M.; Vila, J. M.; Adams, H. J. Organomet. Chem. 2000, 595, 199. (c) Andersen, C.; Crespo, M.; Rochon, F. D. J. Organomet. Chem. 2001, 631, 164. (d) Caubet, A.; Lo´pez, C.; Solans, X.; Font-Bardıá, M. J. Organomet. Chem. 2003, 669, 164. (e) Crespo, M.; Granell, J.; Font-Bardıá, M.; Solans, X. J. Organomet. Chem. 2004, 689, 3088. (f) Wu, Y. J.; Ding, L.; Wang, H. X.; Liu, Y. H.; Yuan, H. Z.; Mao, X. A. J. Organomet. Chem. 1997, 535, 49. (g) Ding, L.; Zou, D. P.; Wu, Y. J. Polyhedron 1998, 17, 2511. (h) Meijer, M. D.; Kleij, A. W.; Lutz, M.; Spek, A. L.; van Koten, G. J. Organomet. Chem. 2001, 640, 166. (i) Kleij, A. W.; Gebbnik, R. J. M. K.; Lutz, M.; Spek, A. L.; van Koten, G. J. Organomet. Chem. 2001, 621, 190. (j) Ryabov, A. D.; Panyashkina, I. M.; Polyakov, V. A.; Fisher, A. Organometallics 2002, 21, 1633. (k) Crespo, M.; Font-Bardıá, M.; Granell, J.; Martıńez, M.; Solans, X. J. Chem. Soc., Dalton Trans. 2003, 3763. (l) Font-Bardıá, M.; Callego, C.; Martıńez, M.; Solans, X. Organometallics 2002, 21, 3305. (m) Avshu, A.; O’Sullivan, R. D.; Parkins, A. W.; Alcock, N. W.; Countryman, R. M. J. Chem. Soc., Dalton Trans. 1983, 8, 1619. (56) Duff, J. M.; Mann, B. E.; Shaw, B. L.; Turtle, B. L. J. Chem. Soc., Dalton Trans. 1974, 139. (57) Jones, Ch. E.; Shaw, B. L.; Turtle, B. L. J. Chem. Soc., Dalton Trans. 1974, 9, 992.


Figure 3. View of complex 4‚1/2CHCl3 with the atomic numbering scheme. Thermal ellipsoids are drawn with 50% probability. The second Pt2 moiety has been omitted for clarity. Intermolecular contacts and hydrogen bonding: Pt1‚‚‚Pt2 3.2871(9) Å, Pt1B‚‚‚Pt2B 3.3140(9) Å, N1-H1 0.88 Å, H1‚ ‚‚O2 2.16 Å, N1‚‚‚O2 2.995(17) Å, N1-H1‚‚‚O2 158.0°, N2-H2 0.88 Å, H2‚‚‚O1 2.15 Å, N2‚‚‚O1 2.991(16) Å, N2-H2‚‚‚O1 159.0°, N1B-H1B 0.88 Å, H1B‚‚‚O2B 2.11 Å, N1B‚‚‚O2B 2.952(16) Å, N1B-H1B‚‚‚O2B 160.4°, N2B-H2B 0.88 Å, H2B‚‚‚O1B 2.14 Å, N2B‚‚‚O1B 2.994(16) Å, N2B-H2B‚‚‚O1B 164.6°.

by IrIII,58 O- and C-metalation of (dimethoxyphenyl)phosphines by PtII and PdII,59 cycloplatination of o-diphenylphosphinebenzaldehyde,60a cyclopalladation of benzylamines,60b cyclometalation of tris(1-pyrazolyl)methane by a PtII center,61 and 1-methyl-2,4′-bipyridinium by PtII and PdII centers.62 Hence, the solid-state conversion of the ligated Ph2CdNH species at the PtII center represents the first example in the chemistry of imines. A significant research effort has been focused on cyclometalated compounds because of the ability of some of them to display interesting photophysical properties.63 In this regard, the cyclometalated PtII complexes64 are among the (58) Smith, L. R.; Blake, D. M. J. Am. Chem. Soc. 1977, 99, 3302. (59) Empsall, H. D.; Heys, P. N.; Shaw, B. L. J. Chem. Soc., Dalton Trans. 1978, 3, 257. (60) (a) Rauchfuss, T. B. J. Am. Chem. Soc. 1979, 101, 1045. (b) Vicente, J.; Saura-Llamas, I.; Palin, M. G.; Jones, P. G.; Ramı´rez de Arellano, M. C. Organometallics 1997, 16, 826. (61) Canty, A. J.; Minchin, N. J. J. Organomet. Chem. 1982, 226, C14. (62) Castan, P.; Labiad, B.; Villemin, D.; Wimmer, F. L.; Wimmer, S. J. Organomet. Chem. 1994, 479, 153. (63) For recent works, see: (a) Bettington, S.; Tavasli, M.; Bryce, M. R.; Batsanov, A. S.; Thompson, A. L.; Al Attar, H. A.; Dias, F. B.; Monkman, A. P. J. Mater. Chem. 2006, 16, 1046. (b) Ott, S.; Borgstroem, M.; Hammarstroem, L.; Johansson, O. J. Chem. Soc., Dalton Trans. 2006, 1434. (c) Laskar, I. R.; Hsu, Sh.-F.; Chen, T.-M. Polyhedron 2006, 25, 1167. (d) Neve, F.; La Deda, M.; Puntoriero, F.; Campagna, S. Inorg. Chim. Acta 2006, 359, 1666. (e) Lo, K. K.W.; Chung, Ch.-K.; Zhu, N. Chem.sEur. J. 2006, 12, 1500. (f) Fang, K.-H.; Wu, L.-L.; Huang, Y.-T.; Yang, Ch.-H.; Sun, I.-W. Inorg. Chim. Acta 2006, 359, 441. (g) Czerwieniec, R.; Kapturkiewicz, A.; Nowacki, J. Inorg. Chem. Commun. 2005, 8, 1101. (h) Tamayo, A. B.; Garon, S.; Sajoto, T.; Djurovich, P. I.; Tsyba, I. M.; Bau, R.; Thompson, M. E. Inorg. Chem. 2005, 44, 8723. (i) Lepeltier, M.; Le Bozec, H.; Guerchais, V.; Lee, T. K.-M.; Lo, K. K.-W. Organometallics 2005, 24, 6069. (j) Mak, C. S. K.; Hayer, A.; Pascu, S. I.; Watkins, S. E.; Holmes, A. B.; Koehler, A.; Friend, R. H. Chem. Commun. 2005, 4708. (k) You, Y.; Park, S. Y. J. Am. Chem. Soc. 2005, 127, 12438. (l) Zhou, G.; Wong, W.-Y.; Bing, Y.; Xie, Z.; Wang, L. Angew. Chem., Int. Ed. 2007, 46, 1149. (m) Wong, W.-Y.; Ho, C.-L.; Gao, Z.-Q.; Mi, B.-X.; Chen, C.-H.; Cheah, K.-W.; Lin, Z. Angew. Chem., Int. Ed. 2006, 45, 7800. (n) Wong, W.-Y.; Zhou, G.-J.; Yu, X.-M.; Kwok, H.-S.; Lin, Z. AdV. Funct. Mater. 2007, 17, 315. (o) Wong, W.-Y.; Zhou, G.-J.; Yu, X.-M.; Kwok, H.-S.; Tang, B.-Z. AdV. Funct. Mater. 2006, 16, 838. (p) Yu, X.-M.; Kwok, H.-S.; Wong, W.-Y.; Zhou, G.J. Chem. Mater. 2006, 18, 5097.

Cyclometalation of Ligated Benzophenone Imine

Figure 4. 1H-13C COSY NMR spectrum of 8 in CD3OD, showing the C2-H2 correlation signal in the aromatic region. Pt satellites in the directly measured one-dimensional 1H and 13C NMR spectra are marked with arrows.

most advantageous owing to such useful features as high efficiency and long lifetimes of the emissive states and potential applications in many fields, e.g., chemosensors65 and light-emitting diodes (LEDs).64g,66 In most cases, the luminescence property is associated with cyclometalated PtII compounds containing various heterocyclic ligands, e.g., pyridine64b,66b,67 and dipyridine,65b,c,67h,68 generally with different aromatic substituents, as well as 7,8-benzoquinoline,64c,67d,69 and aryldiamine64e,f ligands. Surprisingly, nearly no attention was drawn so far to the luminescent cycloplatinated imino species.64a,i In the present work, we observed that the cyclometalated compounds (7-12) obtained exhibit bright-yellow-to-orange luminescence at room temperature in solution, in the solid state, and on being spread onto thin-layer chromatography (TLC) SiO2 plates. Therefore, we conducted a study of their solution and solid-state photophysical properties, and the results are given below in this paper. (64) For recent works, see: (a) Lai, S.-W.; Che, C.-M. Top. Curr. Chem. 2004, 241, 27. (b) Kit-Man Siu, P.; Ma, D.-L.; Che, C.-M. Chem. Commun. 2005, 1025. (c) Diez, A.; Fornies, J.; Garcia, A.; Lalinde, E.; Moreno, M. T. Inorg. Chem. 2005, 44, 2443. (d) Lee, S. J.; Kang, S.; Lee, Jae S.; Lee, S. H.; Hwang, K. J.; Kim, Y. K.; Kim, Y. S. J. Photosci. 2003, 10, 185. (e) Jude, H.; Krause Bauer, J. A.; Connick, W. B. Inorg. Chem. 2005, 44, 1211. (f) Jude, H.; Krause Bauer, J. A.; Connick, W. B. Inorg. Chem. 2004, 43, 725. (g) Ionkin, A. S.; Marshall, W. J.; Wang, Y. Organometallics 2005, 24, 619. (h) Chiu, B. K.-W.; Lam, M. H.-W.; Lee, D. Y.-K.; Wong, W.-Y. J. Organomet. Chem. 2004, 689, 2888. (i) Caubet, A.; Lopez, C.; Solans, X.; FontBardia, M. J. Organomet. Chem. 2003, 669, 164. (j) Che, C.-M.; Fu, W.-F.; Lai, S.-W.; Hou, Y.-J.; Liu, Y.-L. Chem. Commun. 2003, 118. (k) He, Z.; Wong, W.-Y.; Yu, X.; Kwok, H.-S.; Lin, Z. Inorg. Chem. 2006, 45, 10922. (l) Wong, W.-Y.; He, Z.; So, S.-K.; Tong, K.-L.; Lin, Z. Organometallics 2005, 24, 4079. (65) (a) Yang, Q.-Zh.; Wu, L.-Zh.; Zhang, H.; Chen, B.; Wu, Z.-X.; Zhang, L.-P.; Tung, Ch.-H. Inorg. Chem. 2004, 43, 5195. (b) Che, Ch.-M.; Fu, W.-F.; Lai, S.-W.; Hou, Y.-J.; Liu, Y.-L. Chem. Commun. 2003, 118. (c) Ma, Y.-G.; Cheung, T.-Ch.; Che, Ch.-M.; Shen, J.-C. Thin Solid Films 1998, 333, 224. (66) (a) Galbrecht, F.; Yang, X. H.; Nehls, B. S.; Neher, D.; Farrell, T.; Scherf, U. Chem. Commun. 2005, 2378. (b) Cocchi, M.; Virgili, D.; Sabatini, C.; Fattori, V.; Di Marco, P.; Maestri, M.; Kalinowski, J. Synth. Met. 2004, 147, 253. (c) Lu, W.; Chan, M. C. W.; Zhu, N.; Che, Ch.-M.; Li, Ch; Hui, Zh. J. Am. Chem. Soc. 2004, 126, 7639.

Figure 5. View of complex 8 with the atomic numbering scheme. Thermal ellipsoids are drawn with 50% probability. The second Pt molecule in the asymmetric unit has been omitted for clarity.

Characterization and X-ray Structure Determinations of the Cyclometalated PtII Complexes. The cyclometalated complexes 8-12 gave satisfactory elemental analyses and the expected molecular ion/fragmentation patterns in ESIMS spectra (the presence of the [M - Cl]+ and [M + Na]+ peaks was recognized). Complexes 8-12 were characterized by IR spectroscopy: the characteristic ν(SdO) [1116-1126 cm-1], ν(CdN) [1569-1587 cm-1], and ν(NH) [3200-3340 cm-1] bands were observed. The most significant difference of the stretching vibrations between the starting (imine)(sulfoxide)platinum(II) complexes (2-6) and the corresponding cyclometalated products (8-12) was observed for the CdN double bond: the respective absorption band showed a red shift of up to 30 cm-1 in the IR spectrum. In 1H NMR spectra of 8-12, protons H2 displayed satellites deriving from the coupling of the protons with the 195Pt nuclei; typical 3 JPt,H coupling constants between 47.0 and 49.2 Hz could be detected. Coupling of the C2 atoms in complexes 8-12 to 195Pt were also determined in both directly measured 13C NMR and two-dimensional 1H-13C COSY NMR spectra (2JPt,C ) 52.5-61.2 Hz; Figure 4). The presence of the satellites undoubtedly proves the elimination of HCl as a consequence of the cyclometalation process. As expected, a significant difference in δPt was observed between the starting (imine)(sulfoxide)platinum(II) complexes 2-6 (between -1292.3 and -1339.0 ppm) and the corresponding cyclo(67) (a) Koshiyama, T.; Ai, O.; Kato, M. Chem. Lett. 2004, 33, 1386. (b) Williams, J. A. G.; Beeby, A.; Davies, E. S.; Weinstein, J. A.; Wilson, C. Inorg. Chem. 2003, 42, 8609. (c) Liu, Q.; Thorne, L.; Kozin, I.; Song, D.; Seward, C.; D’Iorio, M.; Tao, Y.; Wang, S. J. Chem. Soc., Dalton Trans. 2002, 3234. (d) Lai, S.-W.; Chan, M. C. W.; Cheung, K.-K.; Peng, S.-M.; Che, Ch.-M. Organometallics 1999, 18, 3991. (e) Lai, S.-W.; Chan, M. Ch.-W.; Peng, Sh.-M.; Che, Ch.-M. Angew. Chem., Int. Ed. 1999, 38, 669-671. (f) Balashev, K. P.; Puzyk, M. V.; Kotlyar, V. S.; Kulikova, M. V. Coord. Chem. ReV. 1997, 159, 109. (g) Maestri, M.; Deuschel-Cornioley, Ch.; von Zelewsky, A. Coord. Chem. ReV. 1991, 111, 117. (h) Barigelletti, F.; Sandrini, D.; Maestri, M.; Balzani, V.; von Zelewsky, A.; Chassot, L.; Jolliet, Ph.; Maeder, U. Inorg. Chem. 1988, 27, 3644.


4475


Figure 6. View of complex 10 with the atomic numbering scheme. Thermal ellipsoids are drawn with 50% probability. The other three Pt molecules in the asymmetric unit have been omitted for clarity (see Figure 7).

metalated products 8-12 (between -2240.3 and -2281.7 ppm) because of the change in the ligand sphere (Cl vs C). The crystal structures of two cyclometalated products, i.e., 8 and 10, were determined by X-ray diffraction (Table 1 and Figures 5 and 6). In both structures, the Pt atoms are located at a crystallographic inversion center and display a slightly distorted square-planar coordination. The Pt-Cl bond distances are in the range from 2.381 to 2.397 Å, which is significantly longer compared to those of the corresponding noncyclometalated complexes [2.297-2.308 Å]. The difference in the Pt-Cl bond lengths trans to Cl and trans to C is due to the well-known strong ground-state trans influence of C-bonded ligands.70 However, these distances agree well with those in the previously characterized PtII compounds containing a Cl ligand in the trans position to the platinated C atom.71 In 8 and 10, the coordinated sulfoxide and the platinated C13 center are mutually cis, which is preferable because both centers possess a significant trans influence. The five-membered platinacycles deviate slightly from the plane, with a maximum deviation of 0.149 Å. In 8, the asymmetric unit contains two independent Pt molecules, (68) (a) Siu, K. M.; Lai, S.-W.; Lu, W.; Zhu, N.; Che, Ch.-M. Eur. J. Inorg. Chem. 2003, 2749. (b) Neve, F.; Crispini, A.; Campagna, S. Inorg. Chem. 1997, 36, 6150. (c) Liu, H.-Q.; Cheung, T.-Ch.; Che, Ch.-M. Chem. Commun. 1996, 1039. (d) Wu, L.-Zh.; Cheung, T.-Ch.; Che, Ch.-M.; Cheung, K.-K.; Lam, M. H. W. Chem. Commun. 1998, 1127. (e) Wong, K.-H.; Chan, M. Ch.-W.; Che, Ch.-M. Chem.sEur. J. 1999, 5, 2845. (f) Lai, S.-W.; Cheung, T.-Ch.; Chan, M. C. W.; Cheung, K.-K.; Peng, Sh.-M.; Che, Ch.-M. Inorg. Chem. 2000, 39, 255. (g) Tse, M.-Ch.; Cheung, K.-K.; Chan, M. C.-W.; Che, Ch.-M. Chem. Commun. 1998, 2295. (h) Cheung, T.-Ch.; Cheung, K.-K.; Peng, Sh.M.; Che, Ch.-M. J. Chem. Soc., Dalton Trans. 1996, 1645. (i) Lu, W.; Zhu, N.; Che, Ch.-M. Chem. Commun. 2002, 900. (69) (a) Maestri, M.; Deuschel-Cornioley, Ch.; von Zelewsky, A. J. Photochem. Photobiol. A 1992, 67, 173. (b) Schwarz, R.; Gliemann, G.; Jolliet, Ph.; von Zelewsky, A. Inorg. Chem. 1989, 28, 1053. (c) Fernandez, S.; Fornies, J.; Gil, B.; Gomez, J.; Lalinde, E. J. Chem. Soc., Dalton Trans. 2003, 822. (70) (a) Ryabov, A. D.; Kazankov, G. M.; Yatsimirsky, A. K.; Kuz’mina, L. G.; Burtseva, O. Y.; Dvortsova, N. V.; Polyakov, V. A. Inorg. Chem. 1992, 31, 3083. (b) Ryabov, A. D.; Le Lagadec, R.; Estevez, H.; Hernandez, S.; Alexandrova, L.; Kurova, V. S.; Fisher, A.; Pfeffer, M. Inorg. Chem. 2005, 44, 1626. (71) (a) Ryabov, A. D.; Kazankov, G. M.; Panyashkina, I. M.; Grozovsky, O. V.; Dyachenko, O. G.; Polyakov, V. A.; Kuz’mina, L. G. J. Chem. Soc., Dalton Trans. 1997, 4385. (b) Ryabov, A. D.; Otto, S.; Samuleev, P. V.; Polyakov, V. A.; Alexandrova, L.; Kazankov, G. M.; Shova, S.; Revenko, M.; Lipkowski, J.; Johansson, M. H. Inorg. Chem. 2002, 41, 4286.


Figure 7. Hydrogen-bonding network in structure 10: N1-H1 0.88 Å, H1‚‚‚Cl1B 2.49 Å, N1‚‚‚Cl1B 3.366(4) Å, N1-H1‚‚‚Cl1B 176.0°, N1BH1B 0.88 Å, H1B‚‚‚Cl1 2.55 Å, N1B‚‚‚Cl1 3.426(4) Å, N1B-H1B‚‚‚Cl1 172.9°, N1C-H1C 0.88 Å, H1C‚‚‚Cl1D 2.54 Å, N1C‚‚‚Cl1D 3.416(4) Å, N1C-H1C‚‚‚Cl1D 175.7°, N1D-H1D 0.88 Å, H1D‚‚‚Cl1C 2.38 Å, N1D‚ ‚‚Cl1C 3.262(4) Å, N1D-H1D‚‚‚Cl1C 175.4°.

while in 10, it includes four Pt molecules linked by the intermolecular hydrogen-bonding network between the NH group and Cl atoms (Figure 7). The distances H1‚‚‚Cl1B, H1B‚‚‚Cl1, H1C‚‚‚Cl1D, and H1D‚‚‚Cl1C are 2.49, 2.55, 2.54, and 2.38 Å, respectively, which fall into the range of the typical NH‚‚‚Cl distances when this type of hydrogen bonding takes place.72 Luminescence Studies. Luminescent square-planar PtII complexes have attracted a great deal of interest because of their useful photochemical properties, i.e., high efficiency and long lifetimes of the emissive states and potential applications in many fields, such as chemosensors,73 photocatalysts,74 LEDs,75 and photocatalytic devices.76 The most advantageous d8 PtII luminescent systems are based on [PtX2(diimine)] (X ) halide, cyanide, thiolate, alkyl, aryl, (72) (a) Burrows, A. D.; Harrington, R. W.; Mahon, M. F. Acta Crystallogr. 2004, E60, m1317. (b) Zhu, H.-L.; Yang, S.; Qiu, X.-Y.; Xiong, Z.D.; Youb, Z.-L.; Wang, D.-Q. Acta Crystallogr. 2003, E59, m1089. (73) (a) Lo, H.-S.; Yip, S.-K.; Wong, K. M.-C.; Zhu, N.; Yam, V. W.-W. Organometallics 2006, 25, 3537. (b) Yang, Q.-Z.; Wu, L.-Z.; Zhang, H.; Chen, B.; Wu, Z.-X.; Zhang, L.-P.; Tung, C.-H. Inorg. Chem. 2004, 43, 5195. (c) Che, C.-M.; Zhang, J.-L.; Lin, L.-R. Chem. Commun. 2002, 2556. (74) (a) Du, P.; Schneider, J.; Jarosz, P.; Eisenberg, R. J. Am. Chem. Soc. 2006, 128, 7726. (b) Hissler, M.; McGarrah, J. E.; Connick, W. B.; Geiger, D. K.; Cummings, S. D.; Eisenberg, R. Coord. Chem. ReV. 2000, 208, 115. (c) Connick, W. B.; Gray, H. B. J. Am. Chem. Soc. 1997, 119, 11620. (75) (a) Sotoyama, W.; Satoh, T.; Sawatari, N.; Inoue, H. Appl. Phys. Lett. 2005, 86, 153505. (b) Furuta, P. T.; Deng, L.; Garon, S.; Thompson, M. E.; Frećhet, J. M. J. J. Am. Chem. Soc. 2004, 126, 15388. (76) (a) Chakraborty, S.; Wadas, T. J.; Hester, H.; Schmehl, R.; Eisenberg, R. Inorg. Chem. 2005, 44, 6865. (b) Islam, A.; Sugihara, H.; Hara, K.; Singh, L. P.; Katoh, R.; Yanagida, M.; Takahashi, Y.; Murata, S.; Arakawa, H.; Fujihashi, G. Inorg. Chem. 2001, 40, 5371. (77) (a) Paw, W.; Cummings, S. D.; Mansour, M. A.; Connick, W. B.; Geiger, D. K.; Eisenberg, R. Coord. Chem. ReV. 1998, 171, 125. (b) Miskowski, V. M.; Houlding, V. H.; Che, C.-M.; Wang, Y. Inorg. Chem. 1993, 32, 2518. (c) Che, C.-M.; Wan, K.-T.; He, L.-Y.; Poon, C.-K.; Yam, V. W.-W. J. Chem. Soc., Chem. Commun. 1989, 943. (d) Dungey, K. E.; Thompson, B. D.; Kane-Maguire, N. A. P.; Wright, L. L. Inorg. Chem. 2000, 39, 5192. (e) Wadas, T. J.; Chakraborty, S.; Lachiotte, R. J.; Wang, Q.-M.; Eisenberg, R. Inorg. Chem. 2005, 44, 2628.

Cyclometalation of Ligated Benzophenone Imine Table 2. Photophysical Properties of the Pt Complexes at Room Temperature Solution Data sample 8 9 10 11 12

(dm3 mol-1 cm-1) (λab ) 400 nm)

λem (nm)a

φem (%)b

3400 1600 3100 3900 1400

535, 565 535, 565 535, 565 500-750 535, 565

0.0071 0.019 0.0056 0.0042 0.0045

Solid-State Data sample 8 9 10 11 12

λem (nm)a 542, 571, 624 575, 655 525, 559, 610 600, 655 608, 655

τ (ns)c 455 575 615 323 507

a λ ) 400 nm. b Determined using [Ru(bpy) ]2+ as the standard, φ ) ex 3 0.062 (ref 83). c Excited state (λex ) 400 nm) lifetimes ((50 ns) reported with λem ) 575 nm.

or acetylide),77 terpyridine78 complexes, or phosphorescent platinum(II) porphryins.79 A separate group of PtII-based luminescent compounds is comprised of complexes with N,C,N-67a,75a,80 or S,C,S-80a,81 pincer ligands and some other cyclometalated PtII compounds.64a,82 The UV-vis absorption and emission data of complexes 8-12 are summarized in Table 2 (Attention! For ref 83, see footnote b in Table 2). All of the complexes show an absorption band at 400 nm (Figure 8) with extinction coefficients () on the order of 103 dm3 mol-1 cm-1. These characteristic metal complex absorptions are only reported for λ > 350 nm. Below 350 nm, high-intensity intraligand absorptions predominate in the spectra. The broad but welldefined absorption band at 400 nm may be attributed to a triplet metal-to-ligand charge-transfer (3MLCT) transition corresponding to dπ(Pt) f π*(C∩N), based on similarities in the energy and intensity of MLCT transitions of related platinum(II) terpyridyl and cyclometalated diimine complexes.76a,78,84 In Figure 9, all of the PtII complexes except 11 show an emission with λmax em of 535 nm, along with another less intense emission at 565 nm. Complex 11 has a broad emission ranging from 500 to 650 nm. The solution (78) (a) Yang, Q.-Z.; Wu, L.-Z.; Wu, Z.-X.; Zhang, L.-P.; Tung, C.-H. Inorg. Chem. 2002, 41, 5653. (b) Bailey, J. A.; Hill, M. G.; Marsh, R. E.; Miskowski, V. M.; Schaefer, W. P.; Gray, H. B. Inorg. Chem. 1995, 34, 4591. (c) Wong, K. M.-C.; Tang, W.-S.; Lu, X.-X.; Zhu, N.; Yam, V. W.-W. Inorg. Chem. 2005, 44, 1492. (79) Kwong, R. C.; Sibley, S.; Dubovoy, T.; Baldo, M.; Forrest, S. R.; Thompson, M. E. Chem. Mater. 1999, 11, 3709. (80) Okamoto, K.; Kanbara, T.; Yamamoto, T.; Wada, A. Organometallics 2006, 25, 4026. (81) Kanbara, T.; Okada, K.; Yamamoto, T.; Ogawa, H.; Inoue, T. J. Organomet. Chem. 2004, 689, 1860. (82) (a) Lu, W.; Mi, B.-X.; Chan, M. C. W.; Hui, Z.; Che, C.-M.; Zhu, N.; Lee, S.-T. J. Am. Chem. Soc. 2004, 126, 4958. (b) Kui, S. C. F.; Chui, S. S.-Y.; Che, C.-M.; Zhu, N. J. Am. Chem. Soc. 2006, 128, 8297. (c) Ma, B.; Li, J.; Djurovich, P. I.; Yousufuddin, M.; Bau, R.; Thompson, M. E. J. Am. Chem. Soc. 2005, 127, 28. (83) Calvert, J. M.; Caspar, J. V.; Binstead, R. A.; Westmoreland, T. D.; Meyer, T. J. J. Am. Chem. Soc. 1982, 104, 6620. (84) (a) Lu, W.; Chan, M. C. W.; Cheung, K.-K.; Che, C.-M. Organometallics 2001, 20, 2477. (b) Lai, S.-W.; Chan, M. C.-W.; Cheung, K.K.; Che, C.-M. Organometallics 1999, 18, 3327. (c) Lai, S.-W.; Chan, M. C.-W.; Cheung, T.-C.; Peng, S.-M.; Che, C.-M. Inorg. Chem. 1999, 38, 4046.

Figure 8. Absorption spectra of a 1.0 × 10-5 M solution in acetone at room temperature.

quantum yields of the complexes are rather low, with values smaller than 0.0071, the exception being 9, the quantum yield of which (0.019) is nearly 3 times that of the other compounds. Figure 10 shows normalized solid-state emission spectra for the complexes that exhibit differences with respect to the structure and intensity of the emission bands but have similar emission energies. The solid-state emission data listed in Table 2 show compounds 8 and 10 having λmax em at 571 and 559 nm, respectively. These two complexes also exhibit some structure on the emission bands with high- and lowenergy shoulders at 542 and 624 nm and at 525 and 610 nm, respectively. Complex 9 shows a λmax em at 575 nm with a shoulder at 655 nm. Complexes 11 and 12 exhibit a red shift in the value of λmax em in going from solution to the solid state. It is possible that, in the more rigid solid state, the phenyl rings of the sulfoxide substituent in 11 and 12 have an effect on their solid-state packing arrangement. For compounds 8-12, the excited-state emission lifetimes at 575 nm are in the range of 320-615 ns (Table 2), consistent with the spinforbiddenness associated with metal complex phosphorescence.64c,74b There is no observed correlation of λem and τ. Figure 11 shows the solution emission spectra of 12 at three different concentrations. It is found that the emission intensity increases with increasing concentration but the λmax em energies do not change, consistent with the absence of intermolecular Pt‚‚‚Pt aggregation.82c,85 Though the solidstate quantum yields for the compounds were not obtained, they are indeed very brightly emissive when irradiated with 400 nm light, raising the possibility that these systems may be useful for sensor or display applications, upon proper derivatization. Final Remarks In the current work, we succeeded in synthesizing a new family of orthometalated PtII complexes of the general formula [PtCl{Ph(C6H4)CdNH}(RR′SO)] [R, R′ ) Me, Me; n-Pr, n-Pr; (CH2)4; Me, Ph; Me, p-MeC6H4] (8-12). It was shown that the cyclometalation of trans-[PtCl2(Ph2CdNH)(RR′SO)] (2-6) proceeds both in the solid phase and in a toluene suspension, leading to the formation of N,C-chelates in high isolated yields. Thermogravimetric analysis (TGA) proved to be a perfectly suitable method for the observation of the processes taking place on heating of the solid sample (85) Lai, S.-W.; Lam, H.-W.; Lu, W.; Cheung, K.-K.; Che, C.-M. Organometallics 2002, 21, 226.


4477


Figure 9. Emission spectra of a 1.0 × 10-5 M solution in acetone at room temperature.

Figure 10. Normalized solid-state emission spectra at room temperature.

Figure 11. Emission spectra of 12 in acetone at different concentrations at room temperature (λex ) 400 nm).

at elevated temperatures. It is important that the orthometalated complexes obtained exhibit luminescent properties at room temperature both in solution and in the solid state and also on being spread onto TLC SiO2 plates. The broad application spectrum of luminescent PtII complexes stimulates our interest in the further elaboration of the current topic, and studies on the cyclometalated benzophenone imine complexes and on their emission properties are underway in our group. Experimental Section General Procedures. Solvents were obtained from commercial sources and used as received. n-Propyl sulfoxide was purchased from Acros, while the remaining sulfoxides and benzophenone imine were obtained from Aldrich. The complexes K[PtCl3(RR′SO)] (R, R′ ) Me, Me; n-Pr, n-Pr; (CH2)4; Me, Ph; Me, p-MeC6H4) were prepared in situ according to published methods.46 For TLC, Merck UV 254 SiO2 plates were used. Fluka silica gel 60 (220440 mesh) was used for column chromatography. C, H, and N elemental analyses were carried out by the elemental analyses laboratory of the University of Vienna using a Perkin-Elmer 2400


CHN elemental analyzer. Melting points were determined with a Bu¨chi B-540 melting point apparatus and are uncorrected. TGA/ DTA studies were performed with a Mettler Toledo TGA850 instrument (temperature range from 20 to 1000 °C with a heating rate of 5 °C min-1, an air flow of 3 L h-1, and a sample mass of 5-10 mg in an aluminum crucible; the buoyancy correction for TGA was done by measuring a blank). ESI-MS spectra were obtained with a Bruker Esquire 3000 instrument. IR spectra (4000400 cm-1) were recorded with a Perkin-Elmer Fourier transform (FTIR) instrument in KBr pellets. 1H, 13C{1H}, and 195Pt NMR spectra were measured with a Bruker Avance DPX 400 spectrometer at 400.13 MHz (1H), 100.63 MHz (13C), and 85.99 MHz (195Pt), correspondingly, at ambient temperature. 195Pt chemical shifts are given relative to K2[PtCl4], and the half-height line width is given in parentheses. Reaction of Ph2CdNH with K[PtCl3(RR′SO)] Obtained in Situ. In a typical experiment, a solution of RR′SO (0.25 mmol) in water (1 mL) was added dropwise to a solution of K2[PtCl4] (100 mg, 0.24 mmol) in water (3 mL) at 20-25 °C. The mixture was stirred for 4-5 h at room temperature until the color of the solution turned from reddish-orange to yellow. When Me(Ph)SO and p-MeC6H4(Me)SO were employed, small amounts of the known pale-yellow cis-[PtCl2{Me(Ph)SO}2]46c,86 and cis-[PtCl2{p-MeC6H4(Me)SO}2]87 complexes were obtained and removed by filtration (yields are 10 and 4%, respectively). A solution of Ph2CdNH (44 mg, 0.24 mmol) in CHCl3 (1 mL) was added to the yellow filtrate obtained as described above. A pale-yellow amorphous precipitate appeared immediately, whereupon the reaction mixture was stirred overnight at room temperature and the precipitate was separated by filtration. The yellow solid was dried at 20-25 °C and washed with two 2-mL portions of (86) Antolini, L.; Folli, U.; Iarossi, D.; Schenetti, L.; Taddei, F. J. Chem. Soc., Perkin Trans. 2 1991, 7, 955. (87) Spevak, V. N.; Skvortsov, N. K.; Belskii, V. K.; Konovalov, V. E.; Lobadyuk, V. I. Zh. Obsh. Khim. 1992, 62, 2646.

Cyclometalation of Ligated Benzophenone Imine Table 3. Crystallographic Data for 1, 2, 4‚1/2CHCl3, 8, and 10

empirical formula fw temp (K) λ (Å) cryst syst space group a (Å) b (Å) c (Å) R (deg) β (deg) γ (deg) V (Å3) Z Fcalc (Mg/m3) µ(Mo KR) (mm-1) reflns collected unique reflns R1a (I g 2σ) wR2b (I g 2σ) a

1

2

4

8

10

C26H22Cl2N2Pt 628.45 120(2) 0.710 73 triclinic P1h 9.510(2) 9.680(2) 14.006(3) 70.557(18) 83.699(18) 67.909(12) 1126.3(4) 2 1.853 6.483 6792 3194 0.0351 0.0806

C15H17Cl2NOPtS 525.35 100(2) 0.710 73 monoclinic P21/c 5.5695(5) 16.5381(13) 17.9682(15) 90 98.032(7) 90 1638.8(2) 4 2.129 9.012 22642 3601 0.0201 0.0411

C35H39Cl7N2O2Pt2S2 1222.13 120(2) 0.710 73 monoclinic P21/c 19.869(2) 18.081(3) 23.197(2) 90 99.181(11) 90 8226.8(19) 8 1.973 7.385 57627 14385 0.0631 0.1462

C15H16ClNOPtS 488.89 120(2) 0.710 73 triclinic P1h 10.0666(3) 10.5808(3) 14.7570(3) 107.833(2) 95.223(2) 92.2130(10) 1486.40(7) 4 2.185 9.754 23370 5236 0.0320 0.0719

C17H18ClNOPtS 514.92 120(2) 0.710 73 monoclinic P21 10.38390(10) 24.3071(4) 13.4799(2) 90 99.749(9) 90 3353.23(8) 8 2.040 8.653 54166 15058 0.0231 0.0474

R1 ) ∑||Fo| - |Fc||/∑|Fo|. b wR2 ) [∑[w(Fo2 - Fc2)2]/∑[w(Fo2)2]]1/2.

diethyl ether. The analytically pure products 126 and 2-6 were separated by column chromatography, correspondingly, in the first and second fractions [eluent: 1:8 (v/v) Me2CO/CHCl3]. The products were dried at room temperature. Yield of 1: 6-8%, based on Pt. Yield of 2-6: 40-60%, based on Pt. 1. Anal. Calcd for C26H22N2Cl2Pt: C, 49.69; H, 3.53; N, 4.46. Found: C, 49.52; H, 3.76; N, 4.36. ESI-MS+ (1:10 (v/v) CHCl3/MeOH): m/z 433 [M - HCl - Ph2CdNH + Na]+, 556 [M - HCl - Cl]+, 651 [M + Na]+, 667 [M + K]+. ESI-MS(1:10 (v/v) CHCl3/MeOH): m/z 409 [M - HCl - Ph2CdNH H]-, 446 [M - HCl - Ph2CdNH + Cl]-, 627 [M - H]-, 663 [M + Cl]-. Mp: 212-213 °C. TGA curve, mass loss: 6.4% (-HCl, 200 °C, calcd 5.8%), 18% (310 °C), 37% (410 °C). TLC (20:1 (v/v) CHCl3/Me2CO): Rf ) 0.56. IR (KBr, cm-1): ν 3199 (m, NH), 1591 and 1565 (s, CdN). 1H NMR (acetone-d6): δ 8.89 (s, br, 2H, NH), 8.27 (d, 4H, Har(o), 3JH,H ) 7.0 Hz), 7.80 (t, 2H, Har(p), 3JH,H ) 7.5 Hz), 7.63 (t, 4H, Har(m), 3JH,H ) 7.8 Hz), 7.47 (t, 2H, Har(p), 3JH,H ) 7.3 Hz), 7.25 (t, 4H, Har(m), 3JH,H ) 7.8 Hz), 6.59 (d, 4H, Har(o), 3JH,H ) 7.5 Hz). 13C{1H} NMR (CDCl3): δ 179.08 (CdNH), 137.73 (Car), 136.74 (Car), 132.94 (Car), 132.69 (Car), 130.83 (Car), 129.06 (Car), 128.99 (Car), 128.59 (Car). 195Pt NMR (acetone-d6): δ -240.5 (J ) 660 Hz). Crystals for X-ray study were obtained by slow evaporation of a chloroform/acetone solution. 2. Anal. Calcd for C15H17NCl2OPtS: C, 34.29; H, 3.26; N, 2.66. Found: C, 34.31; H, 3.41; N, 2.40. ESI-MS+ (1:10 (v/v) CHCl3/ MeOH): m/z 490 [M - Cl]+, 548 [M + Na]+, 564 [M + K]+, 671 [M + Ph2CdNH - Cl]+, 706 [M + Ph2CdNH + H]+. ESI-MS(1:10 (v/v) CHCl3/MeOH): m/z 411 [M - Me2SO - Cl]-. Mp: 172 °C. TGA curve, mass loss: 7.5% (-HCl, 160 °C, calcd 7.0%), 21% (310 °C), 42% (450 °C). TLC (8:1 (v/v) CHCl3/Me2CO): Rf ) 0.56. IR (KBr, cm-1): ν 3294 (m, NH), 1599 (m, CdN), 1134 (s, SdO), 702 (s, C-S). 1H NMR (acetone-d6): δ 10.46 (s, br, 1H, NH), 8.15 (d, 2H, 3JH,H ) 7.0 Hz), 7.69 (m, 2H) and 7.59 (m, 6H) (two Ph), 3.29 (s + d, 6H, CH3, 3JPt,H ) 16.6 Hz). 13C{1H} NMR (CDCl3): δ 183.79 (CdNH), 137.83 (Car), 137.13 (Car), 133.48 (Car), 132.83 (Car), 131.48 (Car), 129.85 (Car), 129.34 (Car), 128.28 (Car), 44.04 (CH3). 195Pt NMR (acetone-d6): δ -1339.0 (J ) 550 Hz). Crystals for X-ray study were obtained by slow evaporation of a toluene/dichloromethane solution. 3. Anal. Calcd for C19H25NCl2OPtS: C, 39.25; H, 4.33; N, 2.41. Found: C, 39.20; H, 4.33; N, 2.42. ESI-MS+ (1:10 (v/v) CHCl3/

MeOH): m/z 604 [M + Na]+, 620 [M + K]+, 727 [M + Ph2Cd NH - Cl]+. Mp: 134-135 °C. TGA curve, mass loss: 6.2% (-HCl, 150 °C, calcd 6.3%), 26% (220 °C), 35% (370 °C). TLC (8:1 (v/v) CHCl3/Me2CO): Rf ) 0.61. IR (KBr, cm-1): ν 3195 (m, NH), 1601 (m, CdN), 1113 (s, SdO), 702 (m, C-S). 1H NMR (CDCl3): δ 8.90 (s, br, 1H, NH), 8.12 (d, 2H, 3JH,H ) 7.0 Hz) and 7.58 (m, 8H) (two Ph), 3.53 (td, 2H, 2SCHH, 2JH,H ) 12.6 Hz, 3J 2 3 H,H ) 5.0 Hz), 3.08 (td, 2H, 2SCHH, JH,H ) 11.0 Hz, JH,H ) 5.0 Hz), 2.24 (m, 2H, CH2), 2.13 (m, 2H, CH2), 1.18 (t, 6H, 2CH3, 3J 13C{1H} NMR (CDCl ): δ 184.27 (CdNH), H,H ) 7.5 Hz). 3 133.60 (Car), 132.68 (Car), 131.47 (Car), 129.54 (Car), 129.46 (Car), 128.29 (Car), 56.34 (SCH2), 16.95 (CH2), 13.29 (CH3). 195Pt NMR (CDCl3): δ -1329.1 (J ) 550 Hz). 4. Anal. Calcd for C17H19NCl2OPtS: C, 37.03; H, 3.47; N, 2.54. Found: C, 37.05; H, 3.47; N, 2.54. ESI-MS+ (1:10 (v/v) CHCl3/ MeOH): m/z 516 [M - Cl]+, 574 [M + Na]+, 590 [M + K]+, 697 [M + Ph2CdNH - Cl]+. Mp: 168-169 °C. TGA curve, mass loss: 6.2% (-HCl, 200 °C, calcd 6.6%), 16% (260 °C), 37% (350 °C). TLC (8:1 (v/v) CHCl3/Me2CO): Rf ) 0.49. IR (KBr, cm-1): ν 3227 (m, NH), 1607 (m, CdN), 1129 (s, SdO), 701 (s, C-S). 1H NMR (CDCl3): δ 9.48 (s, br, 1H, NH), 8.16 (d, 2H, 3J H,H ) 7.0 Hz) and 7.56 (m, 8H) (two Ph), 3.96 (m, 2H, SCH2), 3.50 (m, 2H, SCH2), 2.33 (m, 2H, CH2), 2.14 (m, 2H, CH2). 13C{1H} NMR (CDCl3): δ 183.65 (CdNH), 137.84 (Car), 137.16 (Car), 133.40 (Car), 132.78 (Car), 131.49 (Car), 129.86 (Car), 129.31 (Car), 128.26 (Car), 56.82 (SCH2), 25.19 (CH2). 195Pt NMR (CDCl3): δ -1292.3 (J ) 470 Hz). Crystals for X-ray study were obtained by slow evaporation of a chloroform/acetone solution. 5. Anal. Calcd for C20H19NCl2OPtS: C, 40.89; H, 3.26; N, 2.38. Found: C, 40.91; H, 3.41; N, 2.25. ESI-MS+ (1:10 (v/v) CHCl3/ MeOH): m/z 610 [M + Na]+, 626 [M + K]+, 734 [M + Ph2Cd NH - Cl]+. ESI-MS- (1:10 (v/v) CHCl3/MeOH): m/z 441 [M Ph2CdNH + Cl]-. Mp: 162-163 °C. TGA curve, mass loss: 6.9% (-HCl, 180 °C, calcd 6.4%), 14% (260 °C), 43% (370 °C). TLC (20:1 (v/v) CHCl3/Me2CO): Rf ) 0.43. IR (KBr, cm-1): ν 3225 (m, NH), 1599 (s, CdN), 1133 (s, SdO). 1H NMR (acetone-d6): δ 10.62 (s, br, 1H, NH), 8.10 (d, 2H, 3JH,H ) 7.0 Hz), 7.92 (m, 2H) and 7.60 (m, 11H) (three Ph), 3.32 (s + d, 3H, CH3, 3JPt,H ) 12.2 Hz). 13C{1H} NMR (CDCl3): δ 182.79 (CdNH), 143.18 (Car), 137.65 (Car), 137.59 (Car), 133.27 (Car), 132.85 (Car), 132.09 (Car), Inorganic Chemistry, Vol. 46, No. 11, 2007

4479

Scaffidi-Domianello et al. 131.29 (Car), 130.13 (Car), 129.52 (Car), 129.16 (Car), 128.25 (Car), 125.92 (Car), 45.23 (CH3). 195Pt NMR (CDCl3): δ -1334.1 (J ) 520 Hz). 6. Anal. Calcd for C21H21NCl2OPtS: C, 41.94; H, 3.52; N,2.33. Found: C, 41.90; H, 3.45; N, 2.38. ESI-MS+ (1:10 (v/v) CHCl3/ MeOH): m/z 602 [M + H]+, 624 [M + Na]+, 640 [M + K]+. Mp: 164-165 °C. TGA curve, mass loss: 6.3% (-HCl, 190 °C, calcd 6.1%), 6.2% (270 °C), 6.6% (340 °C), 45% (410 °C). TLC (8:1 (v/v) CHCl3/Me2CO): Rf ) 0.70. IR (KBr, cm-1): ν 3198 (m, NH), 1597 (s, CdN), 1131 (s, SdO), 699 (s, C-S). 1H NMR (CDCl3): δ 9.83 (s, br, 1H, NH), 8.10 (d, 2H, H1 and H4, 3JH,H ) 7.0 Hz), 7.90 (d, 2H, H2 and H3, 3JH,H ) 8.1 Hz), 7.66 (m, 1H, Har), 7.62 (m, 2H, 2Har), 7.53 (m, 3H, 3Har), 7.44 (m, 2H, 2Har), 7.38 (m, 2H, 2Har), 3.46 (s, 3H, SCH3), 2.50 (s, 3H, CH3). 13C{1H} NMR (CDCl3): δ 182.84 (CdNH), 143.65 (Car(q)), 140.06 (Car(q)), 137.67 (Car(q)), 137.61 (Car(q)), 133.26 (Car), 132.15 (Car), 131.34 (Car), 130.13 (Car), 130.09 (Car, 3JPt,C ) 87.5 Hz), 129.16 (Car), 128.25 (Car), 125.89 (Car), 45.42 (SCH3), 21.94 (CH3). 195Pt NMR (CDCl3): δ -1318.0 (J ) 450 Hz). Cyclometalation of the Complexed Benzophenone Imine in the Solid State and on Heating in Toluene. The yellow powders of 1 or 2-6 (0.04 mmol) were heated in an open test tube at 180 °C (1), 140 °C (2), 140 °C (3), 180 °C (4), 160 °C (5), or 170 °C (6) overnight, giving a bright-orange product; elimination of HCl was detected by a pH indicator, and weight monitoring proved the loss of 1 equiv of HCl. The yield of 8 was almost quantitative. When 1 and 3-6 were heated, along with cyclometalated complexes 7 and 9-12, the resulting orange solids contained some impurities deriving from decomposition products, as could be detected by 1H NMR spectroscopy. In a typical experiment, suspensions of 1 or 2-6 (0.1 mmol) in toluene (10 mL) were refluxed for 12-16 h, whereupon the solvent was removed at 40 °C under reduced pressure. The bright-orangeyellow powders of 7 or 8-12 were dried in vacuo at room temperature. Yields were almost quantitative. 7. IR (KBr (selected bands), cm-1): ν(CdN) 1594 m [lit.26 IR 1597 m cm-1], ν(CdN) 1578 m [lit.26 IR 1577 m cm-1]. 1H NMR (CDCl3): δ 9.99 (s, br, 1H, NH) [lit.26 δ 10.13], 8.91 (s, br, 1H, NH) [lit.26 δ 8.87], 8.31 (d, 2H, Har, 3JH,H ) 7.3 Hz) [lit.26 δ 8.28 (d)], 7.66 (m, 1H, Har), 7.55 (m, 10H, Har), 7.42 (t, 2H, Har, 3JH,H ) 7.7 Hz) [lit.26 δ 7.35-7.7 (m)], 7.12 (dd, 1H, Har, 3JH,H ) 7.5 Hz, 4JH,H ) 1.6 Hz), 6.97 (m, 2H, Har), 6.85 (d, 1H, Har, 3JH,H ) 7.6 Hz) [lit.26 δ 6.8-7.1 (m)]. In addition, ESI-MS+ analysis was carried out. ESI-MS+ (MeOH): m/z 556 [M - Cl]+, 732 [M + Ph2CdNH - Cl]+.

Me2CO/CHCl3): Rf ) 0.54. IR (KBr, cm-1): ν 3340 (m, NH), 1569 (m, CdN), 1126 (s, SdO). 1H NMR (CD3OD): δ 10.50 (s, br, 1H, NH), 8.20 (d + q, 1H, H2, 3JH,H ) 7.5 Hz, 3JPt,H ) 48.7 Hz), 7.63 (m, 5H, Ph), 7.24 (m, 1H, H3), 7.13 (m, 2H, H4 and H5), 3.55 (s + d, 6H, CH3, 3JPt,H ) 22.1 Hz). 13C{1H} NMR (CD3OD): δ 188.41 (CdN), 145.17 (C1), 134.13 (C2, 2JPt,C ) 54.4 Hz), 133.13 (C3, 3JPt,C ) 50.5 Hz), 131.55 (Car), 131.49 (C5), 128.99 (Car), 128.30 (Car), 124.28 (C4), 45.05 (CH3, 2JPt,C ) 55.4 Hz). 195Pt NMR (CD3OD): δ -2261.7 (J ) 710 Hz). Crystals for X-ray study were obtained by slow evaporation of an acetone solution.

9. Anal. Calcd for C19H24NClOPtS: C, 41.87; H, 4.44; N, 2.57. Found: C, 41.93; H, 4.40; N, 2.55. ESI-MS+ (MeOH): m/z 509 [M - Cl]+, 568 [M + Na]+. Mp: 190-192 °C. TLC (CHCl3): Rf ) 0.44. IR (KBr, cm-1): ν 3206 (w, NH), 1580 (m, CdN), 1116 (s, SdO). 1H NMR (CD3OD): δ 10.43 (s, br, 1H, NH), 8.23 (d + q, 1H, H2, 3JH,H ) 7.5 Hz, 3JPt,H ) 47.2 Hz), 7.63 (m, 5H, Ph), 7.22 (m, 1H, H3), 7.12 (m, 2H, H4 and H5), 3.78 (m, 2H, SCH2), 3.40 (m, 2H, SCH2), 2.17 (m, 2H, CH3CH2), 2.09 (m, 2H, CH3CH2), 1.19 (m, 6H, CH3). 13C{1H} NMR (CD3OD): δ 177.06 (CdN), 144.69 (C1), 135.89 (C6), 134.35 (C2, 2JPt,C ) 52.5 Hz), 132.95 (C3, 3JPt,C ) 51.5 Hz), 132.57 (Car(q)), 131.49 (Car), 131.39 (C5), 128.99 (Car), 128.30 (Car), 124.18 (C4), 57.81 (SCH2, 2JPt,C ) 38.9 Hz), 17.32 (CH2, 3JPt,C ) 22.4 Hz), 12.23 (CH3). 195Pt NMR (CD3OD): δ -2281.7 (J ) 570 Hz).

10. Anal. Calcd for C17H18NClOPtS: C, 39.65; H, 3.52; N, 2.72. Found: C, 39.82; H, 3.65; N, 2.85. ESI-MS+ (MeOH): m/z 538 [M + Na]+, 554 [M + K]+, 590 [M + HCl + K]+. Mp: 173-174 °C. TLC (1:10 (v/v) Me2CO/CHCl3): Rf ) 0.60. IR (KBr, cm-1): ν 3212 (m, NH), 1587 (m, CdN), 1125 (s, SdO). 1H NMR (CD3OD): δ 10.57 (s, br, NH), 8.17 (d + q, 1H, H2, 3JH,H ) 7.5 Hz,

8. Anal. Calcd for C15H16NClOPtS: C, 36.85; H, 3.29; N, 2.86. Found: C, 37.08; H, 3.28; N, 2.86. ESI-MS+ (MeOH): m/z 453 [M - Cl]+, 511 [M + Na]+. Mp: 185-186 °C. TLC (1:10 (v/v) (88) Duisenberg, A. J. M.; Kroon-Batenburg, L. M. J.; Schreurs, A. M. M. J. Appl. Crystallogr. 2003, 36, 220. (89) Otwinowski, Z.; Minor, W. Processing of X-ray Diffraction Data Collected in Oscillation Mode; Academic Press: New York, 1997; pp 307-326. Otwinowski, Z.; Minor, W. Macromolecular Crystallography. In Methods Enzymology; Carter, C. W., Sweet, J., Eds.; Academic Press: New York, 1997; Vol. 276, Part A, pp 307326.


(90) Beurskens, P. T.; Beurskens, G.; Gelder, R.; Garcia-Granda, S.; Gould, R. O.; Israel, R.; Smits, J. M. M. The DIRDIF-99 program system; Crystallography Laboratory, University of Nijmegen: Nijmegen, The Netherlands, 1999. (91) Burla, M. C.; Camalli, M.; Carrozzini, B.; Cascarano, G. L.; Giacovazzo, C.; Polidori, G.; Spagna, R. J. Appl. Crystallogr. 2003, 36, 1103. (92) Sheldrick, G. M. SHELXS-97, Program for Crystal Structure Determination; University of Go¨ttingen: Go¨ttingen, Germany, 1997. (93) Sheldrick, G. M. SHELXTL, Version 6.14-1, Bruker Analytical X-ray Systems; Bruker AXS, Inc.: Madison, WI, 2005. (94) Sheldrick, G. M. SADABSsBruker Nonius scaling and absorption correction, Version 2.10; Bruker AXS, Inc.: Madison, WI, 2003.

Cyclometalation of Ligated Benzophenone Imine Pt,H ) 49.2 Hz), 7.62 (m, 5H, Ph), 7.23 (m, 1H, H3), 7.14 (m, 2H, H4 and H5), 4.15 (m, 2H, CH2), 3.46 (m, 2H, CH2), 2.47 (m, 2H, CH2), 2.31 (m, 2H, CH2). 13C{1H} NMR (CD3OD): δ 185.66 (CdN), 145.26 (C1), 135.74 (C6), 134.51 (C2, 2JPt,C ) 61.2 Hz), 133.89 (Car(q)), 133.17 (C3, 3JPt,C ) 55.4 Hz), 131.58 (Car), 131.54 (C5), 128.99 (Car), 128.34 (Car), 124.28 (C4), 59.54 (2SCH2, 2JPt,C ) 59.3 Hz), 25.95 (2CH2, 3JPt,C ) 28.2 Hz). 195Pt NMR (CD3OD): δ -2240.3 (J ) 730 Hz). Crystals for X-ray study were obtained by slow evaporation of an acetone solution. 3J

11. Anal. Calcd for C20H18NClOPtS: C, 43.59; H, 3.29; N, 2.54. Found: C, 43.44; H, 3.25; N, 2.50. ESI-MS+ (acetone): m/z 515 [M - Cl]+, 574 [M + Na]+, 590 [M + K]+. Mp: 178-180 °C. TLC (1:20 (v/v) Me2CO/CHCl3): Rf ) 0.43. IR (KBr, cm-1): ν 3202 (m, NH), 1581 (s, CdN), 1122 (s, SdO). 1H NMR (acetone-d6): δ 10.17 (s, br, 1H, NH), 8.24 (d, 2H, 2Har, 3JH,H ) 7.8 Hz), 8.05 (d + q, 1H, H2, 3JH,H ) 7.6 Hz, 3JPt,H ) 47.8 Hz), 7.67 (m, 8H, 8Har), 7.16 (m, 1H, H3), 7.09 (m, 2H, H4 and H5), 3.68 (s + d, 3H, CH3, 3JPt,H ) 18.4 Hz). 13C{1H} NMR (acetone-d6): δ 188.41 (CdN), 167.70 (C1), 146.86 (Car(q)), 145.08 (Car(q)), 134.92 (C2, 2JPt,C ) 53.5 Hz), 133.58 (C3, 3JPt,C ) 52.5 Hz), 132.80 (Car), 131.81 (Car), 131.67 (C5, 3JPt,C ) 48.6 Hz), 129.69 (Car), 129.16 (Car), 128.76 (Car), 125.97 (Car), 124.23 (C4), 47.17 (CH3, 2JPt,C ) 42.8 Hz). 195Pt NMR (acetone-d6): δ -2266.1 (J ) 600 Hz).

12. Anal. Calcd for C21H20NClOPtS: C, 44.64; H, 3.57; N, 2.48. Found: C, 44.75; H, 3.65; N, 2.35. ESI-MS+ (MeOH): m/z 529 [M - Cl]+, 588 [M + Na]+. Mp: 169-170 °C. TLC (1:20 (v/v) Me2CO/CHCl3): Rf ) 0.66. IR (KBr, cm-1): ν 3200 (w, NH), 1583 (m, CdN), 1123 (s, SdO). 1H NMR (acetone-d6): δ 10.14 (s, br, 1H, NH), 8.11 (d, 2H, H7 and H10, 3JH,H ) 8.3 Hz), 8.05 (d + q, 1H, H2, 3JH,H ) 7.6 Hz, 3JPt,H ) 47.0 Hz), 7.66 (m, 5H, Ph), 7.49 (d, 2H, H8 and H9, 3JH,H ) 8.1 Hz), 7.16 (m, 1H, H3), 7.09 (m, 2H, H4 and H5), 3.65 (s + d, 3H, SCH3, 3JPt,H ) 18.4 Hz), 2.45 (s, 3H, CH3). 13C{1H} NMR (acetone-d6): δ 191.61 (CdN), 146.91 (Car(q)), 145.68 (Car(q)), 143.57 (Car(q)), 142.09 (Car(q)), 134.93 (C2, 2JPt,C ) 53.5 Hz), 133.93 (Car(q)), 133.56 (C3, 3JPt,C ) 51.5 Hz), 131.80 (Car), 131.64 (C5, 3J Pt,C ) 48.6 Hz), 130.19 (C7 and C10), 129.17 (Car), 128.76 (Car), 125.98 (C8 and C9), 124.18 (C4), 47.33 (SCH3, 2JPt,C ) 43.7 Hz), 20.82 (CH3). 195Pt NMR (acetone-d6): δ -2264.9 (J ) 620 Hz).

X-ray Crystallography. The crystals were immersed in perfluoropolyether, mounted in cryoloops, and measured at 100 or 120 K temperature. The X-ray diffraction data were collected with a Nonius Kappa CCD diffractometer using Mo KR radiation (λ ) 0.71073 Å). The Denzo-Scalepack program or EvalCCD packages88,89 were used for cell refinements and data reductions. The structures were solved by direct methods or by the heavy-atom method using the SHELXS-97 or SIR2002 or the DIFDIF-99 programs, respectively, with the WinGX graphical user interface.90-92 An empirical absorption correction based on equivalent reflections was applied to all data (with XPREP in SHELXTL or with SADABS).93,94 The maximum/minimum transmission factors were 0.3458/0.6932, 0.1842/0.6367, 0.0972/ 0.2271, 0.3095/0.4600, and 0.2530/0.5747 respectively for 1, 2, 4‚ 1/ CHCl , 8, and 10. Structural refinements were carried out with 2 3 SHELXL-97.95 The imine H atoms in 2 were located from the difference Fourier map but constrained to ride on its parent atom [Uiso ) 1.5Ueq (parent atom)]. Other H atoms were positioned geometrically and allowed to ride on their parent atoms, with N-H ) 0.88 Å and Uiso ) 1.2Ueq (parent atom) and C-H ) 0.95-0.99 Å and Uiso ) 1.2-1.5Ueq (parent atom). The asymmetric unit of 4‚1/2CHCl3 contained two dimeric Pt units (four Pt) and one CHCl3 solvent molecule. Structure 8 contained two and structure 10 four Pt moieties in the asymmetric unit. In structure 10, two C atoms (C15D and C16D) were disordered over two positions with occupancies of 0.51 and 0.49. The selected bond lengths and angles are summarized in Table 1 and crystallographic data in Table 3. Luminescence Studies. Absorption spectra were recorded using a Hitachi U2000 scanning spectrophotometer (200-1100 nm). Luminescence spectra were obtained using a Spex Fluoromax-P fluorimeter corrected for the spectral sensitivity of the photomultiplier tube and the spectral output of the lamp with monochromators positioned for a 2 nm bandpass. Excitedstate lifetimes were measured using a Lambda Physik nanosecond laser photolysis system. A Lextra 50 XeCl excimer laser was used to pump 3002 dye laser containing diphenylstilbene, which provided 7 ns, 1 mJ pulses at 400 nm. A monochromator and a fast photomultiplier tube were used to monitor sample emission at 575 nm. For kinetic analysis, the signal from the photomultiplier tube was directed into a Tektronix TDS 620 digitizing oscilloscope and then to a computer for averaging, fitting, and storage. The metal complex concentration of solution samples was 1.0 × 10-5 M, and each sample was degassed by at least three freeze-pump-thaw cycles. Solid-state emission and lifetime samples were prepared as a mixture of the Pt complexes (4.10 × 10-5 mol) in a matrix of finely ground KBr (3.24 × 10-3 mol). All data were recorded at room temperature.

Acknowledgment. Y.Yu.S.-D., M.G., and B.K.K. are indebted to the FWF (Austrian Science Funds) for finan(95) Sheldrick, G. M. SHELXL-97, Program for Crystal Structure Refinement; University of Go¨ttingen: Go¨ttingen, Germany, 1997.


4481

Scaffidi-Domianello et al. cial support. V.Yu.K. and Y.Yu.S.-D. are very much obliged to the Russian Fund for Basic Research (Grants 06-03-90901 and 06-03-32065). V.Yu.K. is grateful to the Scientific Council of the President of the Russian Federation (Grant MK-1040.2005.3) and the Government of St. Petersburg. M.H. and V.Yu.K. are indebted to the Academy of Finland for support of their joint studies (Grant 110465). The authors also acknowledge Paul Merkel for assistance with the excited-state lifetime measurements. The authors gratefully thank Dr. P. Unfried for support with the TGA.


Note Added after ASAP Publication. This article was released ASAP on April 24, 2007. Additional changes were made to Table 1, and the correct version was posted on May 1, 2007. Supporting Information Available: TGA curves of complexes 1-6 as well as crystallographic information files (CIF) of compounds 1, 2, 4, 8, and 10. This material is available free of charge via the Internet at http://pubs.acs.org. IC062414K

First Example of the Solid-State Thermal Cyclometalation of Ligated

Recommend Documents